Patent US4349486A successfully refreshed from Google Patents.
← Back to Patent Explorer
US4349486A Expired / Lapsed US ⏱️ 0.0 years remaining

Monocarbonate transesterification process

Assignee: General Electric Co
•
Filing: 1980-10-31
•
Granted: 1982-09-14
•
Expires: 2000-10-31
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract A monocarbonate transesterification process comprising contacting in the presence of a base, a beta-fluoroaliphatic carbonate and a compound selected from the class consisting of monohydroxy aliphatic alcohols, phenols and ortho-positioned dihydroxy aromatic compounds. The resulting monocarbonates are useful as monocarbonates, per se, or useful in the preparation of polycarbonates which can be molded or formed into films, laminates or reinforced plastics by conventional techniques.

Inventors

  • 👤 Daniel J. Brunelle
  • 👤 William E. Smith

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-08 10:30
CPC Classifications
C; C07; C07C; C07C68/00; C07C68/06; C07C69/00; C07C69/96

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 310 words
A monocarbonate transesterification process comprising reacting, in the presence of a base; (A) a beta-fluoroaliphatic carbonate which is saturated, unsaturated, linear or branched compound of the formula, ##STR14## where R c is selected from the class of a group of the formula, ##STR15## an alkyl radical, a cycloalkyl, aryl radical and combinations thereof which can be carbo-monocyclic, carbo-polycyclic or fused carbo-polycyclic and can have two or more cyclic systems which are connected to each other by a single or double valence bonds or bi- or multi-valent radicals, with (B) a compound selected from the class consisting of (1) monohydroxy aliphatic alcohols of the formula, R.sup.1 OH where R 1 represents an aliphatic radical or cycloaliphatic radical having a single --OH radical attached directly to the aliphatic or cycloaliphatic carbon atom where the alcohol can be a primary, secondary or tertiary alcohol including carbo-monocyclic, carbo-polycyclic or fused carbo-polycyclic alcohol systems which are connected to each other by single or double valence bonds or bi- or multi-valent radicals; (2) monohydroxy phenol R.sub.b OH wherein R b represents an aryl radical having a single --OH radical attached directly to an aryl ring carbon atom wherein the aryl radical can be carbo-monocyclic, carbo-polycyclic, or fused carbo-polycyclic, and can have two or more cyclic systems which are connected to each other by single or double valence bonds or bi- or multi-valent radicals; and (3) an ortho-positioned dihydroxy aromatic compound of the formula, R.sub.c (OH).sub.n wherein R c represents an aromatic radical having at least two --OH radicals ortho-positioned relative to each other, each hydroxy group being directly attached to adjacent aromatic ring carbon atoms, n being a number at least equal to 2 wherein the R c radical can be carbo-monocyclic, carbo-polycyclic, and can have two or more cyclic systems connected to each other by single or double valence bonds, or bi- or multi-valent radicals.
Claim 2
Dependent Claim 310 words
A monocarbonate transesterification process comprising reacting, in the presence of a base; (A) a beta-fluoroaliphatic carbonate which is saturated, unsaturated, linear or branched compound of the formula, ##STR14## where R c is selected from the class of a group of the formula, ##STR15## an alkyl radical, a cycloalkyl, aryl radical and combinations thereof which can be carbo-monocyclic, carbo-polycyclic or fused carbo-polycyclic and can have two or more cyclic systems which are connected to each other by a single or double valence bonds or bi- or multi-valent radicals, with (B) a compound selected from the class consisting of (1) monohydroxy aliphatic alcohols of the formula, R.sup.1 OH where R 1 represents an aliphatic radical or cycloaliphatic radical having a single --OH radical attached directly to the aliphatic or cycloaliphatic carbon atom where the alcohol can be a primary, secondary or tertiary alcohol including carbo-monocyclic, carbo-polycyclic or fused carbo-polycyclic alcohol systems which are connected to each other by single or double valence bonds or bi- or multi-valent radicals; (2) monohydroxy phenol R.sub.b OH wherein R b represents an aryl radical having a single --OH radical attached directly to an aryl ring carbon atom wherein the aryl radical can be carbo-monocyclic, carbo-polycyclic, or fused carbo-polycyclic, and can have two or more cyclic systems which are connected to each other by single or double valence bonds or bi- or multi-valent radicals; and (3) an ortho-positioned dihydroxy aromatic compound of the formula, R.sub.c (OH).sub.n wherein R c represents an aromatic radical having at least two --OH radicals ortho-positioned relative to each other, each hydroxy group being directly attached to adjacent aromatic ring carbon atoms, n being a number at least equal to 2 wherein the R c radical can be carbo-monocyclic, carbo-polycyclic, and can have two or more cyclic systems connected to each other by single or double valence bonds, or bi- or multi-valent radicals.
Claim 3
Dependent Claim 19 words
The process of claim 1 wherein the alcohol is of the formula R'OH and R' is an alkyl radical.
Claim 4
Dependent Claim 19 words
The process of claim 1 wherein the alcohol is of the formula R'OH and R' is an aryl radical.
Claim 5
Dependent Claim 50 words
A monocarbonate transesterification process comprising contacting in the presence of a base, a bis(beta-fluoroaliphatic) carbonate selected from the class consisting of the formulas ##STR16## a monohydroxy-substituted aliphatic or aromatic compound of the formula R.sub.b (OH) where R b is selected from the class consisting of alkyl, cycloalkyl and aryl radicals.
Claim 6
Dependent Claim 50 words
A monocarbonate transesterification process comprising contacting in the presence of a base, a bis(beta-fluoroaliphatic) carbonate selected from the class consisting of the formulas ##STR16## a monohydroxy-substituted aliphatic or aromatic compound of the formula R.sub.b (OH) where R b is selected from the class consisting of alkyl, cycloalkyl and aryl radicals.
Claim 7
Dependent Claim 14 words
The process of claim 4 wherein R b is an C 6-10 aryl radical.
Claim 8
Dependent Claim 18 words
The process of claim 4 wherein R b is a C 1-10 alkyl or C 6-10 cycloalkyl radical.
Claim 9
Dependent Claim 9 words
The process of claim 4 further comprising a solvent.
Claim 10
Dependent Claim 15 words
The process of claim 7 wherein the solvent is a non-, low-, or medium-polar solvent.
Claim 11
Dependent Claim 17 words
The process of claim 8 further comprising separating and recovering a resulting non-fluorinated monocarbonate transesterification reaction product.
Claim 12
Dependent Claim 14 words
The process of claim 5 wherein the monocarbonate transesterification reaction product is diphenyl carbonate.

References Cited (Backward Citations)

US2787632A Cited
US2915529A Cited
US3625920A Cited
US3642858A Cited
US4005121A Cited
DE2615665A1 Cited
US4062884A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1985-09-13 1986-03-15 1986-09-14 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1989-09-13 1990-03-15 1990-09-14 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1993-09-13 1994-03-15 1994-09-14 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag