GB877556A - Purification of a vitamin a intermediate - Google Patents

Purification of a vitamin a intermediate

Info

Publication number
GB877556A
GB877556A GB8756/59A GB875659A GB877556A GB 877556 A GB877556 A GB 877556A GB 8756/59 A GB8756/59 A GB 8756/59A GB 875659 A GB875659 A GB 875659A GB 877556 A GB877556 A GB 877556A
Authority
GB
United Kingdom
Prior art keywords
compound
alkali metal
oxenin
formula
purification
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
GB8756/59A
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.)
Pfizer Inc
Original Assignee
Pfizer Inc
Charles Pfizer and Co Inc
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 Pfizer Inc, Charles Pfizer and Co Inc filed Critical Pfizer Inc
Publication of GB877556A publication Critical patent/GB877556A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/16Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated

Abstract

The invention comprises a compound obtained by the reaction of a compound of formula I <FORM:0877556/IV (b)/1> referred to as oxenin, with an alkali metal hydroxide, one mole of said compound containing from about 1 to about 1.5 moles of alkali metal, and a process for the purification of a compound of formula I which comprises adding an aqueous solution of from about 5% to about 70% by weight of an alkali metal hydroxide to the aforesaid crude compound, recovering the resulting product and treating said product with acid. Crude oxenin is obtained by condensing 2-methyl-4 - (2,6,6 - trimethylcyclohexen-1-yl)-but-2-enal with 3-methylpent-2-ene-4-yne-1-ol in a Grignard reaction. As alkali metal hydroxides there may be used sodium, lithium or potassium hydroxides. Examples illustrate the use of various starting compounds and solvents.
GB8756/59A 1958-04-23 1959-03-13 Purification of a vitamin a intermediate Expired GB877556A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US877556XA 1958-04-23 1958-04-23

Publications (1)

Publication Number Publication Date
GB877556A true GB877556A (en) 1961-09-13

Family

ID=22207057

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8756/59A Expired GB877556A (en) 1958-04-23 1959-03-13 Purification of a vitamin a intermediate

Country Status (1)

Country Link
GB (1) GB877556A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106748943A (en) * 2016-12-30 2017-05-31 厦门金达威维生素有限公司 The method and device that a kind of continuous hydrolysis of the double grignard condensation products of vitamin A intermediate are neutralized
WO2019016315A1 (en) * 2017-07-20 2019-01-24 Dsm Ip Assets B.V. Process of production of 3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-nona-2z,7e-dien-4-yne-1,6-diol

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106748943A (en) * 2016-12-30 2017-05-31 厦门金达威维生素有限公司 The method and device that a kind of continuous hydrolysis of the double grignard condensation products of vitamin A intermediate are neutralized
WO2019016315A1 (en) * 2017-07-20 2019-01-24 Dsm Ip Assets B.V. Process of production of 3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-nona-2z,7e-dien-4-yne-1,6-diol

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