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US4129520A Expired / Lapsed US ⏱️ 0.0 years remaining

Soap making

Assignee: Procter and Gamble Co
•
Filing: 1976-10-12
•
Granted: 1978-12-12
•
Expires: 1996-10-12
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Abstract

Abstract Alkali metal salts of organic acids are prepared by saponifying the corresponding organic acid ester with an alkali metal hydroxide in a liquid reaction medium comprising a substantially water-free alkyl nitrile.

Inventors

  • 👤 Donald J. Peterson

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 17:03
CPC Classifications
C; C11; C11D; C11D13/00; C07; C07C; C07C51/00; C07C51/09; C07C51/41; C07C51/412

Claims Analysis

Total Claims: 17
Claim 1
Independent Claim 101 words
A process for preparing the alkali metal salts of organic carboxylic acids which comprises saponifying the corresponding organic carboxylic acid ester of the formula RCOOR' wherein RCOO- is an organic acid substituent and wherein R' is derived from alcohols or polyols, with an alkali metal hydroxide selected from lithium hydroxide, sodium hydroxide, potassium hydroxide, cesium hydroxide and rubidium hydroxide in a liquid reaction medium comprising a substantially water-free alkyl nitrile of the formula R"CN wherein R" is selected from linear, branched chain, and cyclic aliphatic substituents; separating said salts from the reaction mixture; and removing excess alkyl nitrile from the salts.
Claim 2
Dependent Claim 101 words
A process for preparing the alkali metal salts of organic carboxylic acids which comprises saponifying the corresponding organic carboxylic acid ester of the formula RCOOR' wherein RCOO- is an organic acid substituent and wherein R' is derived from alcohols or polyols, with an alkali metal hydroxide selected from lithium hydroxide, sodium hydroxide, potassium hydroxide, cesium hydroxide and rubidium hydroxide in a liquid reaction medium comprising a substantially water-free alkyl nitrile of the formula R"CN wherein R" is selected from linear, branched chain, and cyclic aliphatic substituents; separating said salts from the reaction mixture; and removing excess alkyl nitrile from the salts.
Claim 3
Dependent Claim 27 words
A process according to claim 1 wherein the alkali metal hydroxide is a member selected from the group consisting of lithium hydroxide, sodium hydroxide, and potassium hydroxide.
Claim 4
Dependent Claim 22 words
A process according to claim 1 wherein the alkyl nitrile is a member selected from the group consisting of acetonitrile and propionitrile.
Claim 5
Dependent Claim 29 words
A process according to claim 1 wherein the organic carboxylic acid ester is a glyceride ester selected from monoglyceride, diglyceride and triglyceride esters of glycerol and organic carboxylic acids.
Claim 6
Dependent Claim 13 words
A process according to claim 4 wherein the glyceride ester is a triglyceride.
Claim 7
Dependent Claim 49 words
A process according to claim 1 for preparing lubricating greases comprising saponifying an organic acid ester wherein the organic acid substituent is a C 10 -C 24 organic acid substituent with lithium hydroxide in a substantially water-free alkyl nitrile reaction medium selected from acetonitrile, propionitrile, butyronitrile, n-pentylnitrile, and cyclohexylnitrile.
Claim 8
Dependent Claim 33 words
A process according to claim 6 wherein the organic carboxylic acid ester is a glyceride ester selected from monoglyceride, diglyceride and triglyceride esters of glycerol and C 10 -C 24 organic carboxylic acids.
Claim 9
Dependent Claim 13 words
A process according to claim 7 wherein the glyceride ester is a triglyceride.
Claim 10
Dependent Claim 22 words
A process according to claim 6 wherein the alkyl nitrile is a member selected from the group consisting of acetonitrile and propionitrile.
Claim 11
Dependent Claim 32 words
A process according to claim 6 wherein the alkyl nitrile is acetonitrile and wherein the ester comprises and mixed glyceride esters derived from animal fats and oils or vegetable fats and oils.
Claim 12
Dependent Claim 55 words
A process according to claim 1 for making soap comprising saponifying an organic carboxylic acid ester wherein the organic acid substituent is a C 10 -C 20 organic acid substituent with sodium hydroxide or potassium hydroxide in a liquid reaction medium comprising a substantially water-free alkyl nitrile selected from acetonitrile, propionitrile, butyronitrile, n-pentylnitrile, and cyclohexylnitrile.
Claim 13
Dependent Claim 33 words
A process according to claim 11 wherein the organic carboxylic acid ester is a glyceride ester selected from monoglyceride, diglyceride, and triglyceride esters of glycerol and C 10 -C 20 organic carboxylic acids.
Claim 14
Dependent Claim 13 words
A process according to claim 12 wherein the glyceride ester is a triglyceride.
Claim 15
Dependent Claim 22 words
A process according to claim 11 wherein the alkyl nitrile is a member selected from the group consisting of acetonitrile and propionitrile.
Claim 16
Dependent Claim 32 words
A process according to claim 11 wherein the alkyl nitrile is acetonitrile and wherein the ester comprises the mixed glyceride esters derived from animal fats and oils or vegetable fats and oils.
Claim 17
Dependent Claim 21 words
A process according to claim 15 wherein the alkyl nitrile is acetonitrile and wherein the alkali metal hydroxide is sodium hydroxide.

References Cited (Backward Citations)

US2753364A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-12-11 1982-06-12 1982-12-12 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-12-11 1986-06-12 1986-12-12 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-12-11 1990-06-12 1990-12-12 $7700.00 Window Closed / Lapsed

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