GB810888A - Therapeutically valuable esters of 3:5:5-trimethylcyclohexanol and mandelic acid, and a process for the preparation thereof - Google Patents
Therapeutically valuable esters of 3:5:5-trimethylcyclohexanol and mandelic acid, and a process for the preparation thereofInfo
- Publication number
- GB810888A GB810888A GB1066/57A GB106657A GB810888A GB 810888 A GB810888 A GB 810888A GB 1066/57 A GB1066/57 A GB 1066/57A GB 106657 A GB106657 A GB 106657A GB 810888 A GB810888 A GB 810888A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mandelic acid
- preparation
- trimethylcyclohexanol
- esters
- alcohol
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/08—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/48—Separation; Purification; Stabilisation; Use of additives
- C07C67/52—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
- C07C67/54—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation by distillation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/732—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids of unsaturated hydroxy carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Emergency Medicine (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises a mixture of esters of 3 : 5 : 5-trimethylcyclohexanol and dl-mandelic acid which consists substantially of esters derived from the low-melting isomer of the alcohol and is completely or substantially free from esters derived from the higher-melting isomer of the alcohol, and the preparation thereof by esterification of 3 : 5 : 5-trimethylcyclohexanol with dl mandelic acid and distilling the crude ester mixture. An example describes the preparation, the distillation being carried out at a pressure of 10 mm. of mercury, while excluding oxygen, the fraction boiling at 184-8 DEG C. being collected.ALSO:The invention includes a pharmaceutical preparation comprising in admixture a mixture of esters of 3 : 5 : 5-trimethyl-cyclohexanol and dl-mandelic acid, which consists substantially of esters derived from the low-melting isomer of the alcohol and is completely or substantially free from esters derived from the high-melting isomer of the alcohol, with a therapeutically suitable vehicle.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL810888X | 1956-01-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB810888A true GB810888A (en) | 1959-03-25 |
Family
ID=19838664
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1066/57A Expired GB810888A (en) | 1956-01-11 | 1957-01-10 | Therapeutically valuable esters of 3:5:5-trimethylcyclohexanol and mandelic acid, and a process for the preparation thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB810888A (en) |
-
1957
- 1957-01-10 GB GB1066/57A patent/GB810888A/en not_active Expired
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2423545A (en) | Esterification of terpene alcohols | |
GB1423118A (en) | Hydrogenation of dmt process residue and distilled dmt process residue | |
GB824595A (en) | Improved method and means for purifying phenol | |
GB903613A (en) | Improvements in or relating to the production of acetoacetic acid esters | |
GB810888A (en) | Therapeutically valuable esters of 3:5:5-trimethylcyclohexanol and mandelic acid, and a process for the preparation thereof | |
US2500005A (en) | Production of esters of unsaturated lower fatty acids | |
GB1352484A (en) | Separation of halogenated alkyl ethers by azeotropic distillation | |
GB965048A (en) | Tetrafluoro-dichloroisopropanol and its hydrate and the production thereof | |
GB1057528A (en) | Process for the manufacture of cyanoacetic acid esters | |
FR1207048A (en) | Process for the preparation of phosphonic esters such as esters of beta-alkoxy- (or beta-alkylmercapto) -vinyl-thiolphosphonic acid | |
US2648664A (en) | 4,4,6-trimethyl-2-(1-hydroxyethyl)-5,6-dihydro-1,3-4h-oxazine | |
US2707193A (en) | 3, 3, 5-trimethyl cyclohexanol-1 mandelate | |
GB827638A (en) | Preparation of citraconic anhydride | |
SU35832A1 (en) | Method for preparing lactone-beta-hydroxy-ethyl acetoacetic acid and gamma-acetopropyl alcohol | |
SU126975A1 (en) | A method of processing Chinese citronella oil | |
GB457859A (en) | Improvements in and relating to the production of phytosterin products | |
GB855696A (en) | Improvements in the preparation of 1-chloro-3-methylbutene-2 | |
GB1262241A (en) | Process for the synthesis of triglycerides | |
SU58217A1 (en) | The method of obtaining reactive varieties of methyl alcohol | |
GB835823A (en) | New derivatives of diphenyl ether and their production | |
GB932153A (en) | New cyclopentanophenanthrene compounds and process for the production thereof | |
Sutherland | The Citronellol Problem and the Isolation of α-Citronellol | |
GB707227A (en) | New esters suitable as medicaments | |
GB1007862A (en) | 4-methyl-6-isobutenyl-pyrone-(2) and a process for its manufacture | |
ES232743A1 (en) | Procedure for the purification of a mixture of esters of 3, 5, 5-trimethyl-cyclohexanol and mandelic acid (Machine-translation by Google Translate, not legally binding) |