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HRID542341

反应详情

EQUATION

反应方程式

HRID 542341 的结构方程式

REACTANTS

反应物

3
结构：CCCCOC(=O)C=C(C)C=CC=C(C)C=Cc1c(C)cc(OC)cc1C
HCID53661015

未命名化合物

结构：CCCCOC(=O)C=C(C)C=CC=C(C)C=O
HCID53845956

Butyl 3,7-dimethyl-8-oxoocta-2,4,6-trienoate

C14H20O3

结构：COc1cc(C)c(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)c(C)c1.[Cl-]
HCID86735899

未命名化合物

PRODUCTS

生成物

1
结构：COc1cc(C)c(C=CC(C)=CC=CC(C)=CC(=O)O)c(C)c1
HCID53899576

未命名化合物

PROCEDURE

实验过程

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.