GB1250204A - - Google Patents
Info
- Publication number
- GB1250204A GB1250204A GB1250204DA GB1250204A GB 1250204 A GB1250204 A GB 1250204A GB 1250204D A GB1250204D A GB 1250204DA GB 1250204 A GB1250204 A GB 1250204A
- Authority
- GB
- United Kingdom
- Prior art keywords
- saccharose
- polar solvent
- ester
- fatty acid
- benzine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
- C07H13/04—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals attached to acyclic carbon atoms
- C07H13/06—Fatty acids
Abstract
1,250,204. Saccharose esters. R. ISMAIL. 11 Dec., 1968 [11 Dec., 1967], No. 58978/68. Heading C2C. Saccharose fatty acid esters are prepared by feeding continuously (1) a solution of saccharose with 0.05-2% by weight'of an alkaline catalyst in a polar solvent and (2) a solution prepared separately of a fatty acid ester derived from a C 12-22 straight chain saturated or unsaturated fatty acid and a C 1-6 aliphatic or cycloaliphatic, mono- or poly-hydric alcohol in an aliphatic or aromatic hydrocarbon or chlorohydrocarbon of boiling point 70-250‹ C. into a reaction cascade which consists of at least three reaction zones connected one after the other in which the reagents are intensively mixed at a temperature 40-150‹ C. and the alcohol liberated in the ester interchange is distilled off under reduced pressure and the mixture issuing from the last reaction zone after a mean residence time of 1-15 hours is sent to a settling vessel, divided in two phases and the polar solvent phase containing the saccharose ester is concentrated by evaporation under reduced pressure in a continuously working drier, and the polar solvent which is liberated in the drier is fed back for re-use earlier in the process. The alkaline catalyst is preferably potassium carbonate, the polar solvent dimethyl sulphoxide and the aromatic hydrocarbons may be benzine. In the examples saccharose and potassium carbonate in dimethyl sulphoxide are reacted with 12-hydroxy-stearic methyl ester in benzine to yield a saccharose ester.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19671668294 DE1668294A1 (en) | 1967-12-11 | 1967-12-11 | Continuous process for the production of sucrose esters of fatty acids |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1250204A true GB1250204A (en) | 1971-10-20 |
Family
ID=5686093
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1250204D Expired GB1250204A (en) | 1967-12-11 | 1968-12-11 |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR1594345A (en) |
GB (1) | GB1250204A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03197442A (en) * | 1989-02-16 | 1991-08-28 | Unilever Nv | Synthesis of polyol fatty acid ester |
US6080853A (en) * | 1996-08-08 | 2000-06-27 | The Procter & Gamble Company | Polyol polyester synthesis |
US6303777B1 (en) | 1990-09-11 | 2001-10-16 | The Procter & Gamble Co. | Process for obtaining highly esterified polyol fatty acid polyesters having reduced levels of difatty ketones and β-ketoesters |
US7304153B1 (en) | 1990-09-11 | 2007-12-04 | The Procter And Gamble Co. | Polyol polyester synthesis |
-
1968
- 1968-12-11 FR FR1594345D patent/FR1594345A/fr not_active Expired
- 1968-12-11 GB GB1250204D patent/GB1250204A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03197442A (en) * | 1989-02-16 | 1991-08-28 | Unilever Nv | Synthesis of polyol fatty acid ester |
US6303777B1 (en) | 1990-09-11 | 2001-10-16 | The Procter & Gamble Co. | Process for obtaining highly esterified polyol fatty acid polyesters having reduced levels of difatty ketones and β-ketoesters |
US7304153B1 (en) | 1990-09-11 | 2007-12-04 | The Procter And Gamble Co. | Polyol polyester synthesis |
US6080853A (en) * | 1996-08-08 | 2000-06-27 | The Procter & Gamble Company | Polyol polyester synthesis |
Also Published As
Publication number | Publication date |
---|---|
FR1594345A (en) | 1970-06-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1515620A (en) | Continuous production of alkyl acrylates free from ether | |
KR970061850A (en) | Process for the continuous production of alkyl esters of (meth) acrylic acid | |
EP0031886B1 (en) | Process for the production of isobutyric acid or its lower alkyl esters | |
GB853983A (en) | Preparation of olefins | |
AR245686A1 (en) | Process for the preparation of dimethyl terephthalate from p-xylene and methanol | |
GB1250204A (en) | ||
US3005846A (en) | Production of acids and esters | |
GB1324440A (en) | Preparation of 2-haloethylphosphonic acids | |
GB1174209A (en) | Process for the preparation of mono-carboxylic acids | |
GB1171273A (en) | Alkane Sulfonic and Percarboxylic Acids | |
GB1483426A (en) | Process for preparing monoalkenylbenzenes | |
US2375629A (en) | Ester of alpha-hydroxy isobutyric acid | |
GB936400A (en) | Process for the manufacture of carboxylic acid-tertiary alkyl esters | |
US3052698A (en) | Ester production | |
US2372221A (en) | Process of acetylating 2,3-butylene glycol with the impure acetic acid obtained from the pyrolytic decomposition of 2,3-butylene glycol diacetate to butadiene | |
US2310762A (en) | Production of aromatic vinyl compounds | |
ES434949A1 (en) | Process for producing ethylphenols | |
GB1226376A (en) | ||
US2626959A (en) | Process for extraction of olefinic hydrocarbon mixtures | |
US2769835A (en) | Process of producing alkyl acrylates by dehydrohalogenation using an anhydrous calcium sulfate catalyst | |
US3127438A (en) | Ester production from isoparaffin and carbon monoxide | |
GB1162899A (en) | Process for the Manufacture of Unsaturated Phosphonic Acid Dichlorides | |
GB1003007A (en) | Improvements in or relating to the production of ethyl acrylate | |
US3201460A (en) | Manufacture of peracetic acid | |
US2849456A (en) | Preparation of dehydroacetic acid |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |