Ethyl 3,7-dimethyl-8-oxoocta-2,4,6-trienoate → HCID 54310465, compound

HRID 27861Notes

Reaction equation

HRID 27861 reaction equation
[Cl-].[Cl:2][C:3]1[C:4]([CH3:32])=[C:5]([C:26]([CH3:31])=[C:27]([Cl:30])[C:28]=1[CH3:29])[CH2:6][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[CH2:33]([O:35][C:36](=[O:47])[CH:37]=[C:38]([CH3:46])[CH:39]=[CH:40][CH:41]=[C:42]([CH:44]=O)[CH3:43])[CH3:34]>>[CH2:33]([O:35][C:36](=[O:47])[CH:37]=[C:38]([CH3:46])[CH:39]=[CH:40][CH:41]=[C:42]([CH3:44])[CH:43]=[CH:6][C:5]1[C:26]([CH3:31])=[C:27]([Cl:30])[C:28]([CH3:29])=[C:3]([Cl:2])[C:4]=1[CH3:32])[CH3:34]

Participants

3

Procedure

3,5-dichloro-2,4,6-trimethyl-benzyl-triphenyl-phosphonium chloride is condensed with 7-formyl-3-methyl-octa-2,4,6-trien-1-oic acid ethyl ester to form 9-(3,5-dichloro-2,4,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid ethyl ester which is converted by the procedure of Example 7 to 9-(3,5-dichloro-2,4,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid, m.p: 220°-222° C.

Sources & evidence

ORD record
ord-024aa1c86dfd4e3991ec0510503107ae
Source dataset
uspto-grants-1980_09
Patent number
US04224244

Reaction notes

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