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Method for synthesizing a salt of a monoester of citric acid

Assignee: Lever Brothers Co
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Filing: 1987-03-10
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Granted: 1989-09-12
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Expires: 2007-03-10
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Abstract

Abstract A skin treatment composition comprising a physiologically acceptable carrier and 1-35% by weight of a salt of a monoester of citric acid. The skin treatment composition imparts a pleasant smoothness to the skin and may be incorporated in several products to treat skin dryness. The hydrophobic group having an ester linkage to citric acid has 10 to 18 carbon atoms. Monoester of citric acid may be synthesized with low levels of di- and triester by forming citric acid anhydride and reacting this to form the monoester.

Inventors

  • 👤 Ira Weil

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 10:42
CPC Classifications
A; A61; A61K; A61K8/00; A61K8/02; A61K8/04; A61K8/046; A61K8/18; A61K8/30; A61K8/33; A61K8/37; A61Q; A61Q19/00; C; C07; C07C; C07C67/00; C07C67/08; A61Q19/007; A61Q19/10

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 235 words
A process for synthesizing a monoester of citric acid comprising: (a) mixing citric acid and an organic anhydride to form a reaction mixture, the organic anhydride having the formula ##STR5## where R 4 and R 5 are independently selected from the group consisting of hydrocarbon chains having from 1 to 5 carbon atoms or, with R 4 and R 5 taken together, having 6 to 8 carbon atoms linked to form a cycloaliphatic or aromatic anhydride or a substituted derivative thereof, and the amount in moles of anhydride being substantially equal to or slightly greater than the amount in moles of citric acid; (b) heating the reaction mixture to at least 60° C. for up to 45 minutes; (c) adding an amount in moles of fatty alcohol to the reaction mixture substantially equal to the amount in moles of the citric acid in the initial reaction mixture, the fatty alcohol having the formula R.sub.1 --OH where R 1 OH is selected from the group consisting of alcohols of the formula R.sub.2 --A--(O--R.sub.3).sub.x --OH (III) or R.sub.2 --(O--R.sub.3).sub.x--OH (IV) where R 2 is a hydrocarbon chain having 10 to 18 carbon atoms, A is an aryl group, R 3 is an alkyl chain having 2 to 4 carbon atoms, and x is an integer from 1 to 7; and (d) heating and continuously distilling the reaction mixture and fatty alcohol forming a monoester of citric acid.
Claim 2
Dependent Claim 235 words
A process for synthesizing a monoester of citric acid comprising: (a) mixing citric acid and an organic anhydride to form a reaction mixture, the organic anhydride having the formula ##STR5## where R 4 and R 5 are independently selected from the group consisting of hydrocarbon chains having from 1 to 5 carbon atoms or, with R 4 and R 5 taken together, having 6 to 8 carbon atoms linked to form a cycloaliphatic or aromatic anhydride or a substituted derivative thereof, and the amount in moles of anhydride being substantially equal to or slightly greater than the amount in moles of citric acid; (b) heating the reaction mixture to at least 60° C. for up to 45 minutes; (c) adding an amount in moles of fatty alcohol to the reaction mixture substantially equal to the amount in moles of the citric acid in the initial reaction mixture, the fatty alcohol having the formula R.sub.1 --OH where R 1 OH is selected from the group consisting of alcohols of the formula R.sub.2 --A--(O--R.sub.3).sub.x --OH (III) or R.sub.2 --(O--R.sub.3).sub.x--OH (IV) where R 2 is a hydrocarbon chain having 10 to 18 carbon atoms, A is an aryl group, R 3 is an alkyl chain having 2 to 4 carbon atoms, and x is an integer from 1 to 7; and (d) heating and continuously distilling the reaction mixture and fatty alcohol forming a monoester of citric acid.
Claim 3
Dependent Claim 50 words
The process for synthesizing a monoester of citric acid according to claim 1 further comprising: (a) cooling the reaction mixture; (b) diluting the reaction mixture; (c) neutralizing the reaction mixture with an organic or inorganic base; and (d) collecting the desalt of the monoester of citric acid as a precipitate.
Claim 4
Dependent Claim 57 words
The process for synthesizing a monoester of citric acid according to claim 1 wherein citric acid is placed in a solvent before the anhydride is added, the solvent being acetone or an acid of the formula R.sub.6 --COOH where R 6 is selected from the group consisting of hydrocarbon chains having from 1 to 5 carbon atoms.
Claim 5
Dependent Claim 22 words
The process for synthesizing a monoester of citric acid according to claim 1 wherein the citric acid used is anhydrous citric acid.
Claim 6
Dependent Claim 80 words
The process for synthesizing a monoester of citric acid according to claim 2 further comprising (a) cooling the reaction mixture to 25° C. or lower after distilling; (b) diluting the reaction mixture with an organic solvent selected from the group consisting of organic alcohols having from 1 to 4 carbon atoms; and (c) neutralizing the mixture to a pH of from 6.0 to 8.5 with organic or inorganic bases while maintaining the reaction mixture temperature at 15° C. or lower.

References Cited (Backward Citations)

US3362923A Cited
US3754860A Cited
US3929870A Cited
US3929712A Cited
US3971626A Cited
EP0199131A2 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1992-09-11 1993-03-13 1993-09-12 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1996-09-11 1997-03-13 1997-09-12 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2000-09-11 2001-03-13 2001-09-12 $7700.00 Window Closed / Lapsed

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