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filingDate 1963-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1967-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1059673-A
titleOfInvention Process for the preparation of polyene compounds
abstract Difficultly crystallizable Vitamin A isomers resulting from the synthetic or extractive preparation of Vitamin A or esters thereof, are reacted with a triaryl phosphine in the presence of a proton donor, or with an acid addition salt of a triaryl phosphine, and the resulting triaryl phosphonium salt is isolated in crystalline form; this salt then may be reacted with an unsaturated aldehyde in the presence of a proton acceptor to obtain a carotenoid. The unsaturated aldehyde may be Vitamin A aldehyde or an aldehyde of formula <FORM:1059673/C2/1> where the bond shown as a broken line is optional, n is 0 or 1 and R is an alkoxycarbonyl or acetalized aldehyde group (see Specifications 1,059,674 and 1,059,675). In examples, retinyl-triphenyl -phosphonium chloride is obtained by reacting triphenyl phosphine with Vitamin A from various sources, and the retinyl-triphenyl-phosphonium chloride is reacted with Vitamin A aldehyde to obtain beta-carotene, with 2,6-dimethyl - 8 - oxo - octatrien - (2,4,6) - acid - (1) ethyl ester to obtain all-trans-b -apo-81-carotenic acid ethyl ester, with 1,1-diethoxy-4-methyl-hexen - (4) - yn - (2 - al - (6) to obtain 111,121-dehydro - b - apo - 101 - carotinal diethyl acetal, with 1,1 - diethoxy - 2,6 - dimethyl - octatrien-(2,4,6)-al-(8) to obtain b -apo-81-carotinal, and with 1,1 - diethoxy - 2,6 - dimethyl - octadien-(2,6) - yn - (4) - al - (8) to obtain 111,121 - dehydro - b - apo - 81 - carotinal diethyl acetal. Reference has been directed by the Comptroller to Specification 877,351.
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priorityDate 1962-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 42.