GB1178423A - Resolution of (±)-Trans-Chrysanthemum-Monocarboxylic Acid Quinine Salt - Google Patents

Resolution of (±)-Trans-Chrysanthemum-Monocarboxylic Acid Quinine Salt

Info

Publication number
GB1178423A
GB1178423A GB09398/67A GB1939867A GB1178423A GB 1178423 A GB1178423 A GB 1178423A GB 09398/67 A GB09398/67 A GB 09398/67A GB 1939867 A GB1939867 A GB 1939867A GB 1178423 A GB1178423 A GB 1178423A
Authority
GB
United Kingdom
Prior art keywords
acid
quinine salt
trans
resolution
chrysanthemum
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
Application number
GB09398/67A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Publication of GB1178423A publication Critical patent/GB1178423A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1,178,423. Resolving (Œ)-trans-chrysanthemum acid. SUMITOMO CHEMICAL CO. Ltd. 27 April, 1967 [27 April, 1966], No. 19398/67. Heading C2C. A process for the resolution of (Œ)-transchrysanthemum monocarboxylic acid comprises adding to a solution thereof in ethanol (at least 500 ml of ethanol per mol of acid being used) at least an equimolar quantity of quinine, separating the (-) acid quinine salt which is precipitated, adding to the mother liquor 45 to 55% of water by volume of ethanol, allowing the mixture to stand and separating the precipitated ( + ) acid quinine salt. Racemic acid may be recovered by adding a large amount of water to the residual mother liquor and decomposing the quinine salt with a mineral acid. The (+) and (-) acid salts are decomposed with a mineral acid to yield the optically pure acid.
GB09398/67A 1966-04-27 1967-04-27 Resolution of (±)-Trans-Chrysanthemum-Monocarboxylic Acid Quinine Salt Expired GB1178423A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2683466 1966-04-27

Publications (1)

Publication Number Publication Date
GB1178423A true GB1178423A (en) 1970-01-21

Family

ID=12204279

Family Applications (1)

Application Number Title Priority Date Filing Date
GB09398/67A Expired GB1178423A (en) 1966-04-27 1967-04-27 Resolution of (±)-Trans-Chrysanthemum-Monocarboxylic Acid Quinine Salt

Country Status (5)

Country Link
CH (1) CH486411A (en)
DE (1) DE1695714C3 (en)
FR (1) FR1522654A (en)
GB (1) GB1178423A (en)
NL (1) NL6705942A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2949384A1 (en) * 1978-12-08 1980-06-26 Roussel Uclaf NEW METHOD FOR CLEAVING THE DL-CIS AND DL-TRANS-CHRYSANTHEMUM ACID

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2949384A1 (en) * 1978-12-08 1980-06-26 Roussel Uclaf NEW METHOD FOR CLEAVING THE DL-CIS AND DL-TRANS-CHRYSANTHEMUM ACID
US4257976A (en) * 1978-12-08 1981-03-24 Roussel Uclaf Resolution process using L or D N-methyl-ephedrine

Also Published As

Publication number Publication date
CH486411A (en) 1970-02-28
DE1695714B2 (en) 1973-11-08
DE1695714C3 (en) 1974-06-20
DE1695714A1 (en) 1972-04-13
NL6705942A (en) 1967-10-30
FR1522654A (en) 1968-04-26

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