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US4112235A Expired / Lapsed US ⏱️ 0.0 years remaining

Transesterification of carboxylic acids

Assignee: Honeywell UOP LLC
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Filing: 1976-10-28
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Granted: 1978-09-05
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Expires: 1996-10-28
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Abstract

Abstract Carboxylic acids may be esterified by reaction with esters in the presence of a catalytic amount of a tin halide catalyst, the reaction being effected at temperatures ranging from about 0° to about 150° C.

Inventors

  • 👤 Louis Schmerling

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 05:17
CPC Classifications
C; C07; C07C; C07C67/00; C07C67/10; C07C2601/00; C07C2601/12; C07C2601/14; Y; Y02; Y02P; Y02P20/00; Y02P20/50; Y02P20/582

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 106 words
A transesterification process which comprises reacting, in the presence of a catalytic amount of stannic chloride, bromide or iodide at a temperature in the range of from about 0° to about 150° C. and a pressure in the range of from about atmospheric to about 100 atmospheres, a carboxylic acid selected from the group consisting of fatty acids of from 1 to about 20 carbon atoms, cycloalkanecarboxylic acids having from 5 to 8 carbon atoms in the ring and aromatic carboxylic acids with an alkyl, cycloalkyl, unsaturated aliphatic, cycloaliphatic or benzyl formate, acetate, butyrate, acrylate, crotonate, oleate or benzoate, and recovering the resultant esterified carboxylic acid.
Claim 2
Dependent Claim 106 words
A transesterification process which comprises reacting, in the presence of a catalytic amount of stannic chloride, bromide or iodide at a temperature in the range of from about 0° to about 150° C. and a pressure in the range of from about atmospheric to about 100 atmospheres, a carboxylic acid selected from the group consisting of fatty acids of from 1 to about 20 carbon atoms, cycloalkanecarboxylic acids having from 5 to 8 carbon atoms in the ring and aromatic carboxylic acids with an alkyl, cycloalkyl, unsaturated aliphatic, cycloaliphatic or benzyl formate, acetate, butyrate, acrylate, crotonate, oleate or benzoate, and recovering the resultant esterified carboxylic acid.
Claim 3
Dependent Claim 16 words
The process as set forth in claim 1 in which the catalyst is anhydrous stannic chloride.
Claim 4
Dependent Claim 16 words
The process as set forth in claim 1 in which the catalyst is stannic chloride pentahydrate.
Claim 5
Dependent Claim 15 words
The process as set forth in claim 1 in which the catalyst is stannic bromide.
Claim 6
Dependent Claim 28 words
The process as set forth in claim 1 in which said acid is propionic acid, said ester is allyl acetate and said esterified carboxylic acid is allyl propionate.
Claim 7
Dependent Claim 28 words
The process as set forth in claim 1 in which said acid is propionic acid, said ester is vinyl acetate and said esterified carboxylic acid is vinyl propionate.
Claim 8
Dependent Claim 28 words
The process as set forth in claim 1 in which said acid is phthalic acid, said ester is allyl acetate and said esterified carboxylic acid is allyl phthalate.
Claim 9
Dependent Claim 28 words
The process as set forth in claim 1 in which said acid is crotonic acid, said ester is benzyl benzoate and said esterified carboxylic acid is benzyl crotonate.
Claim 10
Dependent Claim 28 words
The process as set forth in claim 1 in which said acid is cyclohexanecarboxylic acid, said ester is butyl acrylate and said esterified carboxylic acid is butyl cyclohexanecarboxylate.

References Cited (Backward Citations)

US2931819A Cited
US1691425A Cited
US3714234A Cited
US3649655A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-09-04 1982-03-06 1982-09-05 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-09-04 1986-03-06 1986-09-05 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-09-04 1990-03-06 1990-09-05 $7700.00 Window Closed / Lapsed

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