Note : Les descriptions sont présentées dans la langue officielle dans laquelle elles ont été soumises.
11~3989~
Field of the Invention
-
The present invention relates to methods for preparing
sterically hindered bis- or polyphenols which are useful as
effective non-colorating, non-toxic and low-volatile stabilizing
agents for rubbers, vulcanizates, plastics and other organic
products.
Said stabilizing agents can be exemplified by such a
well known compound as 2,2'-methylene-bis-(4-methyl-6-tert.
butylphenol) produced under the trade marks "~ntioxidant 2246~,
KAO -5, and the like.
Backqround of the Invention
Known in the art are various methods for preparing
sterically hindered bisphenols of polyphenols. For example,
currently used is a method for preparing 2,2'-methylene-bis-(4-
methyl-6-tert.butylphenol), wherein the desired product is
prepared by alkylation of 4-methylphenol with isobutylene in the
presence of a catalyst, followed hy separation and condensation
of the resulting 2-tert.butyl-4-methylphenol with formaldehyde.
Condensa~ion is conducted in the presence of acidic ca-
talysts such as sulphuric acid. The process is carried outin an aqueous emulsion containing a surfactant and an organic
solvent at a temperature within the range of from 75 to 90C.
This prior art method has a disadvantage residing in a
complicated technology of the process.
q~
-3-
11(~9894
Tha process is performed in two stages, a great amount
o~ waste w3ters i8 formed (about 30 m3 per to~ o~ the product)
which are contami~ated wit~ ~ur~aota~t~ and orga~iC solve~ts.
Besides~ a8 the starting product i~ the process use is made
of p-cresol which is di~ficult to obtain.
Due to p-cresol bei~g a critical product, anothex
met~od ~or the preparation o~ 2,2'-methyle~e-bis-(4-methyl-6-
-tert.butylphenol) from 2~6-ditert.but~1-4-m~thylphenol ha~
been developed, based on t~e production o~ the latter ra-ther
readily ~rom cheap and easily available phe~ol. The process
is based on dealkylatio~ of 2,6-di~ert.butyl-4-methylphenol,
~ollowed by separatio~ a~d co~deusation o~ the re~ulti~g
2-tert butyl-4-met~ylphenol with formaldehyde.
One of principal disad~antageE of tbis method also re-
eides in the formatiou of a great amount of acidic waste
waters co~taining surfactants a~d or~anic solve~ts. Puri~i-
cation of suc~ waste waters on a commercial scale is rather
complicated and eco~omically ine~ficient.
Also know~ in t~e art is a method for prepari~g 2,2'-
methylene-bis(4-methyl-6-tert.butylphenol) which has certain
advautages over t~e methods me~tio~ed hereinabo~e, since it
makes possibls to elimi~ate the formation o~ waste waters.
Acoordi~g to this method, t~e desired product is obtained
~rom 2,6-ditert~butyl 'I-methylphenol ~ two sta~es, namely:
dealkylation o~ 2,6-ditert.butyl-4-methylphenol, ~ollowed by
I
1~09~94
separation and condensation of the result ng 2--tert.b-utyl-
4-methylphenol with an acetal in the pres~nce of a~ acidic
catalyst a~ a temperature within the ran$e of from 30 to
14() C .
~ his prior art process as well as those described here-
i~before are two-sta~ed and require separation, in pure
form, of 2-tert.butyl-4-methylphe~ol havin~ a stro~g un-
pleasant odour, high toxicity a~d volatility. Further~iore,
a complicated process technology is required to perform all
the above-discussed prior art methods.
Moreover, the prior art methods described hereinbefore
make it possible to prepare snly bisphenols. A8 regards poly-
phenols, know~ in the art are complicated multi-staged meth-
ods of preparing same. For example, polyphenols are prepared
by reacting paraalkylphenols with free ortho-pssitionq with
chloromethyl derivatives of 2,6-dialk~lphe~ols according to
th~ followi~g scheme:
t _
~(C~ C~ , C~
~ J.s OJ3Ae ~ ~
Ou rC~ ~ C~c~sJ~
Sn C~4
C'(CIJ3)~ ~zC~ C r~3)~'
~(cU . ) OH
C~c/4~)3
~ 8 9'~
Brie~ Summary of the I~vent on
It is a main object of the pres~nt invention to simplify
the process technology.
It is another object of the prese~t invention to incre-
ase the desired product ~ield and quality as well as improve
sanitar~ and hygienic co~ditio~s o~ work for th~ perso~nel-
~ he main a~d other objects of the present inventio~ areaccomplished by that in the ~erein-proposed method for prepa-
ri~g sterically hingered bis- or polyphenols of the formula:
R" - ~X - R"'
Rl
wherei~ R' i5 hydrogen or a C1-C4 alkyl~ R" and R"' bei~g
either th~ same or different a~d each representing:
Q o~ Q C~ ~ q
~, o~ ~, C~ 40 ~C~ ~
~2
~herein R is a tertiary C4-C8 alkyl, R1 and ~ ar~ the same
or di~ferent and represe~t a C1-C8 al~yl or a C6-C8 cycloal- :
kyl, or a C7-C9 aralkyl, i~ wbich met~od according to the
prese~t i~vention the starti~g sterically hindered 2,4,6-trial-
kylphenols o~ the ~ormula:
0
B
--6--
" : :
9 8 9 ~
~herein A is a C1-C~ alkyl or a C6-C~ cycloalkyl, or a C7-Cg
aralkyl or a 3,5-dialkyl-2-hydroxybenzyl of th~ ~ormula:
0~
~ ~ C~-
Q1
B is a C1-C8 alkyl~ olr a C6-C8 cycloalkyl, or a C7-C9 ~ral-
B kyl, or a 3,5 ~ ~4-hydroxybe~zyl o~ the ~ormula: Q~
~,~ '
C'f2 -
wherei~ R is a tertiary C4-C8 alkyl, R1 is a C1-C~ al~yl, or
a C6-C8 cycloaLkyl, or a C7-C9 aralkyl,
are reacted with acetals, aldehyde~ or donors of C1-&5
aldehydes in a~ acidic medium at a temperature within the
ra~Oe of ~rom 60 to 200C i~ the prese~ce of an acidi¢ ca-
talyst, followed by isolatiou of the desired product.
As the acidic catalysts it is pre~erable to use 3rnstedt
acids such as qulphuric acid, ortho-phosphoric acid, polyphos-
phoric acid, perchloric acid, toluenesulphonic acid, ~aptha-
leuesulphonic acid, catio~ite~ in H+ form a~d the like, or
Iewis acids suc~ as i~c chloride, alumlDium chloride, ~erric
chloride, boro~ tri~luoride and the like. ~hese catalysts
axe readily separated ~rom the desired produ~t an~ e~ure
a hioh yield thereo~, i.e. at least 78.7~ of t~e reacted
starti~g 2~4,6-trialkylphe~ols, predomi~antl~ at least 95%
of the theoretical yield.
. -7-
11~98~d~
As the acetals use is preferably made of commonly avail-
able and simple in handling compounds of the formula:
R3-0(-CH-O~)n - R3, wherein R3 is Cl to C5 alkyl and
R4
R4 is hydrogen or Cl to C4 alkyl, n = 1 to 4.
Certain acetals comprise waste products from other
syntheses, in particular, methylal is a waste product from the
synthesis of isoprene rubber. Most preferable among acetals are
methylal, ethylal, dipentylformal, however, use may be made of
other acetals such as dimethylacetal, diethylacetal, diisopropyl-
acetal and the like.
As aldehydes it is preferred to use acetaldehyde, pro-
pionic aldehyde, butyric aldehyde, isobutyric aldehyde, valeric
aldehyde, isovaleric aldehyde, because these comprise readily
available and easy-to-handle reagents. It is also possible to
use formaldehyde and other aldehydes.
As donors of Cl-C5 aldehydes in an acidic medium use can
be made of cyclic polymers of aldehydes such as trioxane, paral-
dehyde, 2,4,6-tri-isobutyl-1,3,5-trioxane, since these products
are more stable upon storage and easier to handle as compared to
monomeric aldehydes.
Among cyclic polymers trioxane is most preferred, since
most valuable antioxidants are those sterically hindered bis-
or polyphenols which have methylene bridges between aromatic
rings.
As donors of C1-C5 aldehydes in an acidic medium use
--8--
l39~
ca~ be also made of lin~ar polymers of aldehydes~ since the
latter polymers just as cyclic polymers o~ aldehydes, are
more stable upo~ s-torage. Paxaform is the most preferred
linear polymeric ~ldehyde, since it, like trioxane, ensures
incorporatior~ o~ methylene bridges in between aromatic ri~s
thus providing ~or the formation of most valuable methylene-
bisphenols or methylene-polyphenol~.
Detailed Disclosure of the Inventio~
The method according to the presant invention is per
~ormed in the following manner.
Into a four-neck reactor provided with a stirrer, ther-
mometer, cooler, and a heating bath there are charged a steri-
cally hindered 2,4,6-trialkylphe~ol such as 2,6-ditert. butyl-
-4-methylphenol, a~ acidic catalyst such as sulphuric acid or
a cationite i~ H+ -form, or zinc chloride and the mi~ture is
heated to a predatermined temperature under stirring. While
maintai~in3 thifi temperature, into tke reactor, still under
stirri~g for 0.5 - 2 hours, there is ~ed an acetal such as
methylal, or a~ aldehyde such as acetaldehyde, or a donor of
a C1-C5 aldehyde in an acidic medium, such as paraform.
The process temperature is maintained within tha ranve
of from 60 to 200C. On completio~ o-~ the process~ the ca-ta-
lyst is separated a~d the desired product is isolated by con-
ventio~al techniques such as, for example, crys~allizatio~.
_9_
llQ9894
The yield of the desired products is as high as 78.7
to 99.1% of the theoretical, as calculated for the reacted ste-
rically hindered 2,4,6-trialkylphenol, predorninantly above 95%;
for the most effective stabilizing agent, i.e. 2,2'-methylene-
bis-(4-methyl-6-tert.butylphenol) the yield is as high as 97.8-
99.1%. The method according to the present invention ensures
the production of high-quality compounds. Thus, melting point
of 2l2'-methylene-bis(4-methyl-6-tert.butylphenol) prepared by
the method of the present invention is 131-131.5C (according to
the literature data, m.p. of the product is 131-132C)~
The method according to the present invention features
certain advantages over the prior art methods. The selected re-
actants and conditions of interaction thereof ensure the pro-
duction of the desired bisphenols or polyphenols from sterically
hindered 2,4,6-trialkylphenols in a single stage, wherefore
the process technology is substantially simplified and the
sanitary and hygienic conditions of labour are improved, since no
pure 4-methyl-2-tert.butylphenol possessing high toxicity, strong
unpleasant odour and high volatility is evolved in the process.
High-quality products are obtained in the process requiring no
additional crystallization. Bis-phenols or polyphenols can be
obtained from monophenols following the method according to the
present invention, by appropriately selecting the reaction condi-
tions. The unreacted starting products are recycled back into the
process. ~le
-1.0-
-
~110989~
tertiary olefines resulting from t~e reaction are u ed in
the preparation o~ the starti~g sterically hindered 2,4,6-
trialkylphenols. ~he method according to the prese~t invention
completely eliminates the formation of waste ~aters and atmosp-
here pollutants.
For a better understanding of the present inve~tion,
some spcci~ic examples illustrating the method for preparin~
sterically hindered bis- and polyphenols are ~iven hereinbelow.
Example 1
Into a reactor provided with a stirrer, thermometer and
a heating bath there are charged 220 g (1g.-mol) of 2,6-di-
tert.butyl 'I-methylphenol~ 2.2. g of concentrated sulphuric
acid and the mixture is heated to the temperature o~ 12~C.
i~hile maintaini~g the temperature at 120C, 94 g (1.24 g-mol)
of methylal are ~ed into the reactor for 1.5 hour. On comp-
letion of t~e reaction, the catalyst is separated, volatile
products are distilled under vacuum to give 143.0 g o~ 2,2'-
methylene-bi~4-methyl-6-tert.butylphenol) which corresponds
to 97~% of theory calculated ~or the reacted 2,6-ditert.butyl
-4-methylphe~ol (co~version degree o~ the latter is 86.0~).
A~ter a single recrystallizatio~ the resulting product
has ~t~ melti~ point of 131-131.5C ~rom the literature
data m.p. is 131-132C).
~ he unreacted 2,6-ditert.buty~-4-methylphenQl and methyl-
al are recycled back into the proce~s.
8 9
~ample 2
Into a relctor similar to that d~scribed in F~ample 1
hereinabove there are charged 22~ g (1 ~-mol) of 2,6-ditert.-
~utyl-4-methylphenQl, 2~2 g o~ co~centrated sulphuric acid
and at the temperature of 1~C 76 g (1.0 g-mol) of ~thylal
are fed i~to the reactor for 1 hour. The reaction mass is trea-
ted following the procedure described in the ~oregoing Exa~ple
1 to give 112.9 g of 2,2'-methylene-bis-(4-methyl-6 tert.butyl-
phenol) which co~stitute~ 99.1% o~ theory, as calcula~ed for
the reacted 2,6-dltert.butyl-4-methylphenol (conversion o~ th~
latter is 67.0O . ~he u~reacted methylal and 2~6-ditert.butyl-
-4-methylphe~ol are recyclad back into the process.
Example 3
Into the reactor described in the foregoi~g Example 1
t~ere are charged 220 g (1.0 g-mol) of 2,6-ditert.butyl-4-
methylpheuol, 2.2 g o~ sulphuric acid and 44 g (1 g-mol) of
acetaldehyde are fed i~to the reactor ~or one hour at the
temperature of 125C. 0~ completio~ o~ t~e reaction, the
reaction mass is treated ~ollowi~g the procedure described
in tha ~oregoing Example 1 to give 124.6 g of 1,1,-(5-methyl-
3-tert.butyl-2-hydroxypheuyl)etha~e which constitutes 95.4%
of theory, as calculated for the reacted 2,6-ditert.butyl-4-
-methylphenol (couversion o~ the latter iP 73%).
A~ter a single recrystallization the resultinæ product
has its melting poi~t of 1U4-104.5C (~ro~ the literature
data m.p. o~ the product i~ 104.5C).
-12-
11~398~4
The unroac-ted 2,6-ài~ert.bu~yl-4-met~ylphenol a~d acct-
aldehyde are recycled back i~to the process.
~ xample 4
Into the reactor de~cribed i~ Ex~mple 1 hereinbefore
there are char~ed 212 g (0~5 g-mol) of 4,4'-m~thylene-bis-
(2,6-ditert.butylphenol), 8.4 g of zinc chloride and 10 g
(O.111 g-mol) of trioxane are added to the mixturé o~er 3
minutes at the temp~ra~ure o~ 200C. On completion of the
reaction, the catalyst is separated, volatile products are
distilled u~der vacuum to give 193.7 g o~ 2,2'-methylene-
bis- ~4-(3,5-ditert.butyl-4-hydrox~benzyl)-6-tert.butylpheno~
i~ the form o~ a resi~ having molecular wei~ht of 736 (the
theoretical molecular wei~ht o~ the condensation product is
748)-
Example 5
Into the reactor described in the foregoing Example~there are charged 170 g (0.5 g-mol) of 2,2'-methylene-bis-
(4-meth~1-6-tert.butylphenol), 34 g of a cation-exchange
resi~ in H+-form (sulp~onated copolymer o~ styrene with
diYinylbenzene) a~d at tha temperature of 16~C 8.2 g (~.26
g-mol) of para~orm (calculated for the 95% product) are
added to the reaction ~ass over one hour. On completion of
~he reactio~, the catalyst is separated, volatile products
are distilled u~der vacuum to ~i~e 141.9 g o~ a resi~ con-
taining 46.1% by weight o~ the condensat~on product, i.e.
2,2' methylene-bis- r4-methyl-6~(3-tert.butyl-5-methyl-2-
-13-
1~U~ 8~
hydroxybenzyl~phcnol~ a~d 53 9% by wcight of t~e starti~g
product. ~he thus-obtain~d resin can be used a8 a~ antioxi-
da~t.
Exal~ple 6
Into the reactor d~scribed in Example 1 herein~efore
there are charged 282 g (1 g-mol) o~ 2,4,6-tritert.butylp~enol,
9 g o~ a concentrated sulphuric acid and 110 g (1.17 g-mol)
of dipentylformal are i~troduced into the reactor over 2
hours at the temperature of 60C. On completio~ of the reac-
tion, the catalyst is separated, volatile products are distil-
led under vacuum to give 120.7 g of the desired prcduct, i.e.
2,2'-methylene-bis-(4,6-ditert.butyl_phenol) ~hich constitu-
tes 98.2% of t~eory, as calculated ~or the reacted 2,4,6-
tritert.but7lphenol (conversion of the latter is 53%).
After a single recrystallizatio~ the re~ulting product
has its melting poi~t o~ 141-142C.
~ he u~reacted 2,4,6-tritert.butylphenol and dipe~tyl-
~ormal are recycled back into tho process.
Example 7
I~to t~e reactor described i~ Example 1 hereinbefore the-
re are charged 155 g (0.5 g-mol) of 2,6-ditert.butyl-4- ~ -
methylbenzene,phenol, 3.2 g o~ para-toluenesulpho~ic acid and
21.9 g (0.255 ~-mol) of isovaleric aldehyde are added thereto
at the temperature o~ 150C over 1.5 hour. 0~ completio~ of
the reaction, the catalyst is separated, volatile products
are distilled under vacuum to give 12Q.9 ~ of 1,1-(6-tert.
butyl-4- ~-methylbe~zylphe ol)i~opentane which corresponds to
-14-
.
1~9894
95.8% of theory, as calculated ~or the reacted 2,6-ditert.
butyl-4~ ethylbenzylphenol (conversio~ of the latter is ~0)
~ample 8
In~o the reactor described i~ ~ampla 1 hereinbefore
there are charged ~30 g (1. 5 g-~ol) ol 2,~-d~ ~r~.butyl-4-
methylphenol, 6. 5 g o~ concentrated sulphuric acid and 152 g
(2 g-mol~ o~ ~ethylal are added thereto over 2 hours at the
temp0rature of 150C. On completion o~ the react~on, the cata-
lyst is separated, volatile products are distilled under ~a-
cuu~ to give 200.3 ~ of the desired product, i.e. 2,6-di-~5-
-methy1-3-tert.butyl-2 hydro~ybenzyl)-para-cresol which co~s-
titutes 87.1~ of tbe theory as calculated ~or the reacted
2,6-ditert.butyl-4-met~ylp~enol (co~versio~ of tbe latter is
1 00%) ~
After recrystallizatlo~ the thus-prepared product has
its melti~g point of 163-163.5C.
Example 9
Into the reactor described in Example 1 there are char-
~d 22~ g (1Ø g-mol) of 2,6-ditert.buty~-4-methylphenol,
11 g o~ ortho-phops~oric acid and 66 g (1.5 g-mol) o~ acetal-
dehyde are added there-to at the temperature o~ 150C over
one hour. On co~pletion Q~ the reactiou, the catalyst is se-
parated, volatile products are distilled under ~acuu~ to
gi~e 210 ~ o~ a ~ixture of 1,1-(5-met~y1-3-tert.butyl-2-h~d-
roxyphenyl)ethane and 2~6-di-(5-m~t~yl-3-tert.butyl-2-~ydro-
Yymet~lbenzy:~para-cresol. ~e resultir~ mixture can be used
-1 5-
.
1~39894
without any separatio~ as an antioYidant. Co~version of 236-
ditert . butyl~-methy~phenol i8 99%.
Example 10
Into th~ reactor described in Example 1 hereinbefore
there are charged 12~ g (0.5 g mol) o~ 2-tert.butyl-6~c~clo-
~exyl 'I-~ethylphenol, 42.2 g o~ a concentrated sulphuric
acid and the mixture is heated at the tempera~ure o~ 120C
Then at this temperature 47 g (1.12 g-mol~ of m~thylal are
added into the reactor over 1.5 hour. On completio~ of the
reaction, the catalyst is separ~ted, volatile products are
distilled under vacuum to give 163.1 g o~ 2,2'methylene-
bis-(4-methyl-6-cyclohexylphenol) which constitute~ 99.1%
of theory, as calculated ~or the reacted 2-tert.butyl-6-cyclo-
hexyl 'I-methylphenol (conversion o~ the latter is 84%).
After recrystallization the resulti~g produot has its
melting point of 117-117.5C.
~ he unreacted 2-tert.butyl-6-cyclo~exyl-4-methylphenol
and methylal are recycled bac~ into the process.
Exa~ple 11
Into the raactor described in Example 1 hereinbe~ore
there are charged 159 g (0.5 g-mol) of 2,6-ditert.butyl-4-
tert.octylphenol, 2 g o~ concentrated sulphuric acid and
36 g (0.5 g-mol) o~ bu~yric aldehyde are added into the reac-
tor at the temperature o~ 125C over one hour. 0~ completion
o~ the reaction, the catalyst is separated, volatile products
are distilled under vacuum to give 1~.3 g of the desired pro-
-16-
389~
dllct, i.e. 1,1-(3-tert.butyl-5-tert.octyl-2-hydroxyphenyl)butane
which corresponds to 95.3% of theory, as calculated for the
reacted 2,6-ditert.bl1tyl-4-tert.octylphenol (conversion of the
latter is 75.0%).
Ihe unreacted 2,6-d;tert.butyl-4-tert.octylphenol and
hutyric alclehyde are recycled back into the process.
Example 12
Into the reactor described in Example 1 hereinbefore
there are charged 234 g (1 g-mol) of 2-tert.octyl-4,6-xylenol,
~,4 g of a concentrated sulphuric acid and 76 g (1 g-mol) of
methylal are added thereto at the temperature of 100C over
one hour. I~e reaction mass is treated following the procedure
of the foregoing Example 11 to give 63.5 g of the desired product,
i.e. 2,2'-methylene-bis-(4,6-dimethylphenol) which constitutes
81.1% of the theoretical yield as calculated for the reacted
2-tert.-octyl-4,6-xylenol (conversion of the latter is 61.2%).
The unreacted 2-tert.octyl-4,6-xylenol and methylal are
recycled back into the process.
Example 13
Into the reactor described in Example 1 hereinbefore
there are charged 58.5 g (0.25 g-mol) of 2,6-ditert.butyl-
4-ethylphenol, 1 g of a concentrated sulphuric acid and 19 g
(0.25 g-mol) of methylal are added into the reactor at the
temperature of 130C over 30 minlltes. The reaction mass is
treated and 26.2 g of 2,2'-methylene-bis-(4-ethyl-6-tert.butyl-
phenol) are thus obtained which corresponds to 98.9% of the
theoretical yield calculated for the reacted 2,6-ditert.butyl-
-4-ethylphenol (CQnversion of the latter is 57.5).
.~,
~ -17-
98g~
After a single recrystallization a product is obtained
which melts at 124.5-125.0C.
The unreacted 2,6-ditert.butyl-4-ethylphenol and methyl-
al are recycled back into the process.
Example 14
Into the reactor described in the foregoing Example 1
there are charged 141.0 g (0.5 g-mol~ of 2-tert.butyl-4-methyl-
6-cumylphenol, 1.5 g of a concentrated sulphuric acid and 52 g
(0.5 g-mol) of eth~lal are added to the mixture at the temper-
ature of 130C for one hour. On completion of the reaction, the
catalyst is separated, the unreacted 2-tert.butyl-4-methyl-6-
cumylphenol and ethylal are distilled under vacuum to give 62.5
g of the desired product, i.e. 2,2'-methylene-bis-(4-methyl-6-
cumylphenol) which constitutes 78.7% of the theoretical yield
calculated for the reacted 2-tert.butyl-4-methyl-6-cumylphenol
(conversion of the latter is 68.5%). The unreacted products
are recycled back to the process.
Example 15
Into the reactor described in the foregoing Example 1
there are charged 70.5 g (0.25 g-mol) of 2-tert.hexyl-4-methyl-
-6-benzylphenol, 20 g of a cation-exchange resin in H -form
(sulphonated copolymer of styrene with divinylbenzene) and 17.4
g ( b . 3 g-mol) of propionic aldehyde are added into the reactor
at the temperature of 145C over 30 minutes. On completion of
the reaction, the catalyst is separated, volatile products are
distilled under vacuum to give 31.4 g of 1,1-(5-methyl-3-
benzyl-2-hydroxyphenyl)propane which constitutes 91.1% of the
theoretical yield calculated for the reacted 2-tert.hexyl-4-
-18-
methyl-benzylphenol (conversion of the latter is 63.2%).
The unreacted 2-tert.hexyl-4-methyl-6-benzylphenol and
propionic aldehyde are recycled back to the process.
-19-
