FR2091396A5 - Dopa optical resolution by selective crystallization from superstaura - Google Patents

Dopa optical resolution by selective crystallization from superstaura

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Publication number
FR2091396A5
FR2091396A5 FR7116770A FR7116770A FR2091396A5 FR 2091396 A5 FR2091396 A5 FR 2091396A5 FR 7116770 A FR7116770 A FR 7116770A FR 7116770 A FR7116770 A FR 7116770A FR 2091396 A5 FR2091396 A5 FR 2091396A5
Authority
FR
France
Prior art keywords
isomer
dopa
supersatd
soln
superstaura
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
FR7116770A
Other languages
French (fr)
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.)
KH Neochem Co Ltd
Original Assignee
Kyowa Hakko Kogyo 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
Priority claimed from JP4050870A external-priority patent/JPS5136260B1/ja
Priority claimed from JP6027270A external-priority patent/JPS5136261B1/ja
Application filed by Kyowa Hakko Kogyo Co Ltd filed Critical Kyowa Hakko Kogyo Co Ltd
Application granted granted Critical
Publication of FR2091396A5 publication Critical patent/FR2091396A5/en
Expired legal-status Critical Current

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

Abstract

The optical isomers of DL-(3,4-dihydroxyphenyl)alanine (dopa) are produced by preparing a supersatd. acidic to neutral solution of dopa which contains an excess of one of the two optical isomers and, after partial crystallisation has taken place, isolating the precipitated isomer by conventional methods. The isomer which is present in excess crystallises selectively from the supersatd. soln., and if the crystallisation is interrupted at an appropriate point may be isolated in pure form. One advantageous way of carrying out the procedure is to seed a supersatd. soln. of DL-dopa with crystals of the desired isomer. After separation of the crystallised isomer there is obtained a soln. in which the other isomer predominates, and this soln. can be supersatd. and the procedure repeated for this other isomer. L-Dopa is of use in the treatment of Parkinsonism, but the D-isomer is inactive.
FR7116770A 1970-05-14 1971-05-10 Dopa optical resolution by selective crystallization from superstaura Expired FR2091396A5 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP4050870A JPS5136260B1 (en) 1970-05-14 1970-05-14
JP6027270A JPS5136261B1 (en) 1970-07-11 1970-07-11

Publications (1)

Publication Number Publication Date
FR2091396A5 true FR2091396A5 (en) 1972-01-14

Family

ID=26379971

Family Applications (1)

Application Number Title Priority Date Filing Date
FR7116770A Expired FR2091396A5 (en) 1970-05-14 1971-05-10 Dopa optical resolution by selective crystallization from superstaura

Country Status (2)

Country Link
DE (1) DE2123114A1 (en)
FR (1) FR2091396A5 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5518905A (en) * 1993-07-30 1996-05-21 Ajinomoto Co., Inc. Method for producing L-3,4-dihydroxyphenylalanine by precipitation of anhydrous crystals

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5518905A (en) * 1993-07-30 1996-05-21 Ajinomoto Co., Inc. Method for producing L-3,4-dihydroxyphenylalanine by precipitation of anhydrous crystals

Also Published As

Publication number Publication date
DE2123114A1 (en) 1971-11-25

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