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GB868482A - Process for the preparation of 8ª--hydroxy-2ª--methoxy-3ª-,5ª--epoxy 1,2,3,4,4aª-,5,8,8aª--octahydronaphthalene-1ª--carboxylic acid lactone and intermediates obtained therein - Google Patents

Process for the preparation of 8ª--hydroxy-2ª--methoxy-3ª-,5ª--epoxy 1,2,3,4,4aª-,5,8,8aª--octahydronaphthalene-1ª--carboxylic acid lactone and intermediates obtained therein

Info

Publication number
GB868482A
GB868482A GB548/59A GB54859A GB868482A GB 868482 A GB868482 A GB 868482A GB 548/59 A GB548/59 A GB 548/59A GB 54859 A GB54859 A GB 54859A GB 868482 A GB868482 A GB 868482A
Authority
GB
United Kingdom
Prior art keywords
methoxy
epoxy
carboxylic acid
octahydronaphthalene
hydroxy
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
GB548/59A
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.)
Laboratoires Francais de Chimiotherapie SA
Original Assignee
Laboratoires Francais de Chimiotherapie SA
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 Laboratoires Francais de Chimiotherapie SA filed Critical Laboratoires Francais de Chimiotherapie SA
Publication of GB868482A publication Critical patent/GB868482A/en
Expired legal-status Critical Current

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

Abstract

The lactone of 8b -hydroxy-2a-methoxy-3b ,5b -epoxy- 1,2,3,4,4aa ,5,8, 8aa -octahydronaphthalene-1b -carboxylic acid <FORM:0868482/IV (b)/1> is made by converting the bromohydrins derived from the mother liquor of crystallisation from the 1,8-lactone of 6a -bromo-7b ,8b -dihydroxy-2a -methoxy-3b ,5b -epoxy- 4aa ,8aa , decahydronaphthalene-1b -carboxylic acid into their tosylates by the action of tosyl chloride in the presence of a tertiary base, and subjecting the resulting mixture of tosylates to reduction with zinc and an aliphatic acid containing 1 to 8 carbon atoms in the presence of an inert organic solvent, The invention also relates to the tosylates of a mixture of two bromohydrins, of which one melts at Ca.158 DEG to Ca.160 DEG C. and the other melts at Ca.184 DEG C., and which bromohydrins are isomeric with the compound of the formula: <FORM:0868482/IV (b)/2> Specifications 868,475 and 868,483 are referred to. Reference has been directed by the Comptroller to Specification 799,269.
GB548/59A 1958-01-09 1959-01-06 Process for the preparation of 8ª--hydroxy-2ª--methoxy-3ª-,5ª--epoxy 1,2,3,4,4aª-,5,8,8aª--octahydronaphthalene-1ª--carboxylic acid lactone and intermediates obtained therein Expired GB868482A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR868482X 1958-01-09

Publications (1)

Publication Number Publication Date
GB868482A true GB868482A (en) 1961-05-17

Family

ID=9346157

Family Applications (1)

Application Number Title Priority Date Filing Date
GB548/59A Expired GB868482A (en) 1958-01-09 1959-01-06 Process for the preparation of 8ª--hydroxy-2ª--methoxy-3ª-,5ª--epoxy 1,2,3,4,4aª-,5,8,8aª--octahydronaphthalene-1ª--carboxylic acid lactone and intermediates obtained therein

Country Status (1)

Country Link
GB (1) GB868482A (en)

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