9-(4-Methoxy-2,6-dimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid butyl ester → 9-(4-Methoxy-2,6-dimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid
Reaction equation
C([O:5][C:6](=[O:27])[CH:7]=[C:8]([CH3:26])[CH:9]=[CH:10][CH:11]=[C:12]([CH3:25])[CH:13]=[CH:14][C:15]1[C:20]([CH3:21])=[CH:19][C:18]([O:22][CH3:23])=[CH:17][C:16]=1[CH3:24])CCC.[Cl-].COC1C=C(C)C(C[P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=C(C)C=1.C(OC(=O)C=C(C)C=CC=C(C=O)C)CCC>>[CH3:23][O:22][C:18]1[CH:17]=[C:16]([CH3:24])[C:15]([CH:14]=[CH:13][C:12]([CH3:25])=[CH:11][CH:10]=[CH:9][C:8]([CH3:26])=[CH:7][C:6]([OH:27])=[O:5])=[C:20]([CH3:21])[CH:19]=1Participants
4
Reactant 3
Product 1
Procedure
By the procedure described in Example 14, 9-(4-methoxy-2,6-dimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid butyl ester is manufactured from 4-methoxy-2,6-dimethylbenzyl-triphenylphosphonium chloride by reaction with 7-formyl-3-methyl-octa-2,4,6-trien-1-oic acid butyl ester. From this product, there is produced by the procedure of Example 15, 9-(4-methoxy-2,6-dimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid of melting point 207°-208° C.
Sources & evidence
- ORD record
- ord-ab8a0fa60fd0461c8f40c150fa7a2e1f
- Source dataset
- uspto-grants-1985_07
- Patent number
- US04532355
Reaction notes
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