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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904455Generated: October 30, 2026

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

https://huagongshe.com/reaction/904455

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantTriethylamineHCID 8471—
Reactant3-Formyl-crotonic acid butyl esterHCID 86735241—
SolventWaterHCID 962—
ProductButyl 3,7-dimethyl-8-oxoocta-2,4,6-trienoateHCID 53845956—

Reaction Conditions

Temperature25 °C

Reaction Steps

212.6 G. of 2-formyl-but-2-ene-4-triphenyl-phosphonium chloride and 95 g. of 3-formyl-crotonic acid butyl ester are introduced into 1100 ml. of butanol and treated at 5° C. with a solution of 57 g. of triethylamine in 60 ml. of butanol. The reaction mixture is subsequently stirred for 6 hours at 25° C., then cooled and introduced into water and thoroughly extracted with hexane. The hexane phase is washed first repeatedly with methanol/water (6:4 parts by volume), then with water, dried over sodium sulphate and filtered. The filtrate is isomerized for 12 hours by shaking with iodine. The iodine is removed by the addition of sodium thiosulphate. The filtrate is washed again with water, dried and evaporated under reduced pressure. The remaining 7-formyl-3-methyl-octa-2,4,6-trien-1-oic acid butyl ester boils, after rectification, at 102°-105° C./0.09 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04230872
Source datasetuspto-grants-1980_10
ORD IDord-2e952843b8cb42f1aaebe30b4d752ec7
Source noteuspto-grants-1980_10