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Process for the preparation of carbonic acid diesters containing at least one aromatic ester group

Assignee: Bayer AG
•
Filing: 1991-02-20
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Granted: 1992-09-22
•
Expires: 2011-02-20
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Abstract

Abstract Aromatic and aliphatic-aromatic carbonic acid diesters can be obtained by transesterification of carbonic acid diesters containing aliphatic ester groups if polymeric hydroxystannoxanes are employed as catalysts.

Inventors

  • 👤 Norbert Schon
  • 👤 Hans-Josef Buysch
  • 👤 Wolfgang Ebert

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 13:27
CPC Classifications
C; C07; C07C; C07C68/00; C07C68/06

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 122 words
A process for the preparation of carbonic acid diesters containing at least one aromatic ester group from the reaction of carbonic acid diesters containing at least one aliphatic ester group and phenols by catalysed transesterification, wherein one or more polymeric hydroxystannoxanes containing monomeric units of the formula ##STR14## in which R 1 denotes straight-chain or branched C 1 -C 18 -alkyl, C 3 -C 8 -cycloalkyl, C 6 -C 14 -aryl, C 7 -C 15 -aralkyl or a C 1 -C 18 -alkylene radical or C 6 -C 14 -arylene radical bridging two polyhydroxystannoxane chains, are employed as the catalyst in an amount of 0.001-20% by weight, based on the carbonic acid diester employed which contains at least one aliphatic ester group.
Claim 2
Dependent Claim 122 words
A process for the preparation of carbonic acid diesters containing at least one aromatic ester group from the reaction of carbonic acid diesters containing at least one aliphatic ester group and phenols by catalysed transesterification, wherein one or more polymeric hydroxystannoxanes containing monomeric units of the formula ##STR14## in which R 1 denotes straight-chain or branched C 1 -C 18 -alkyl, C 3 -C 8 -cycloalkyl, C 6 -C 14 -aryl, C 7 -C 15 -aralkyl or a C 1 -C 18 -alkylene radical or C 6 -C 14 -arylene radical bridging two polyhydroxystannoxane chains, are employed as the catalyst in an amount of 0.001-20% by weight, based on the carbonic acid diester employed which contains at least one aliphatic ester group.
Claim 3
Dependent Claim 36 words
The process of claim 1, wherein one or more polymeric hydroxystannoxanes containing monomer units of the formula ##STR15## in which R 2 denotes straight-chain or branched C 3 -C 12 -alkyl, phenyl or benzyl, are employed.
Claim 4
Dependent Claim 33 words
The process of claim 2, wherein one or more polymeric hydroxystannoxanes, containing monomer units of the formula ##STR16## in which R 3 denotes straight-chain on branched C 3 -C 8 -alkyl are employed.
Claim 5
Dependent Claim 17 words
The process of claim 1, wherein the catalyst is employed in an amount of 0.005-5% by weight.
Claim 6
Dependent Claim 17 words
The process of claim 4, wherein the catalyst is employed in an amount of 0.005-2% by weight.
Claim 7
Dependent Claim 65 words
The process of claim 1, wherein a carbonic acid diester containing at least one aliphatic ester group, of the formula R.sup.4 O--CO--OR.sup.5 in which R 4 and R 5 independently of one another denote straight-chain or branched C 1 -C 12 -alkyl or C 3 -C 8 -cycloalkyl, and wherein R 4 can furthermore denote substituted or unsubstituted C 6 -C 12 -aryl, is employed.
Claim 8
Dependent Claim 59 words
The process of claim 6, wherein a carbonic acid diester containing at least one aliphatic ester group, of the formula R.sup.6 O--CO--OR.sup.7 in which R 6 and R 7 independently of one another denote straight-chain or branched C 1 -C 8 -alkyl, cyclopropyl, cyclopentyl or cyclohexyl, and wherein R 6 can furthermore denote substituted or unsubstituted phenyl, is employed.
Claim 9
Dependent Claim 138 words
The process of claim 1, wherein a phenol of the formula ##STR17## in which R 8 denotes hydrogen, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 1 -C 4 -alkoxy, C 5 -C 6 -cycloalkyl, phenyl, fluorine, chlorine, bromine, cyano or nitro; R 9 represents hydrogen, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 1 -C 4 -alkoxy, fluorine, chlorine or bromine and represents hydrogen, C 1 -C 4 -alkyl or the group ##STR18## in which X denotes a single bond, --CH 2 --, C 2 -C 5 -alkylene, C 2 -C 5 -alkylidene, C 5 -C 6 -cycloalkylene, C 5 -C 6 -cycloalkylidene, oxygen, sulphur, --CO--, --SO-- or --SO 2 --, or wherein R 9 and R 10 together can also denote a fused-on benzene nucleus, is employed for the transesterification.
Claim 10
Dependent Claim 48 words
The process of claim 8, wherein a phenol of the formula ##STR19## in which R 11 and R 12 independently of one another denote hydrogen, C 1 -C 4 -alkyl , C 5 -C 6 -cycloalkyl or chlorine, and wherein R 11 can additionally denote nitro, is employed.
Claim 11
Dependent Claim 83 words
The process of claim 8, wherein a bisphenol of the formula ##STR20## in which R 13 and R 14 independently of one another denote hydrogen, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 1 -C 4 -alkoxy, C 5 -C 6 -cycloalkyl, fluorine, chlorine or bromine, and wherein R 13 can additionally denote nitro, and Y represents a single bond, --CH 2 --, C 2 -C 5 -alkylidene, C 5 -C 10 -cycloalkylidene, sulphur or --SO 2 -- is employed.
Claim 12
Dependent Claim 31 words
The process of claim 10, wherein a bisphenol of the formulae ##STR21## in which R 13 , R 14 and Y have the meaning as indicated in claim 10, is employed.
Claim 13
Dependent Claim 15 words
The process of claim 1, which is carried out at a temperature of 50°-300° C.
Claim 14
Dependent Claim 15 words
The process of claim 12, which is carried out at a temperature of 100°-250° C.
Claim 15
Dependent Claim 14 words
The process of claim 1, wherein the polymeric hydroxystannoxane has 3-30 recurring polymeric units.
Claim 16
Dependent Claim 14 words
The process of claim 14, wherein the polymeric hydroxystannoxane has 3-20 recurring polymeric units.
Claim 17
Dependent Claim 15 words
The process of claim 1, which is carried out at a pressure of 0.5-50 bar.
Claim 18
Dependent Claim 15 words
The process of claim 16, which is carried out at a pressure of 1-10 bar.

References Cited (Backward Citations)

DE2736062A1 Cited
DE3445552A1 Cited
DE3445555A1 Cited
US4554110A Cited
EP0338760A2 Cited
US5034557A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1995-09-22 1996-03-23 1996-09-22 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1999-09-22 2000-03-23 2000-09-22 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2003-09-22 2004-03-23 2004-09-22 $7700.00 Window Closed / Lapsed

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