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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259206Generated: October 29, 2026

Triphenylphosphine → 3-Ethoxypropionylmethylenetriphenylphosphorane

https://huagongshe.com/reaction/259206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-Chloro-4-ethoxybutan-2-oneHCID 14068889—
SolventChloroformHCID 6212—
Product3-EthoxypropionylmethylenetriphenylphosphoraneHCID 2054292253.3%

Reaction Steps

A solution of 1-chloro-4-ethoxybutan-2-one (7.5 g.) and triphenylphosphine (13.5 g.) in chloroform (20 ml.) was saturated with nitrogen and heated at reflux under nitrogen overnight. The chloroform was removed in vacuo and the residue was dissolved in dichloromethane (35 ml.). Dry diethyl ether (300 ml.) was added to precipitate 4-ethoxy-2-oxobutyltriphenylphosphonium chloride (19 g.). This compound was added portionwise to a solution of sodium carbonate (10g.) in water (1000 ml.) and the mixture was stirred vigorously for 24 hours. The solution was extracted with diethyl ether, and the ethereal extracts were dried over magnesium sulphate. The solvent was removed by evaporation and the residue was cooled and triturated with petroleum ether (b.p. 60°-80° C.) to give 3-ethoxypropionylmethylenetriphenylphosphorane (10.0 g.), m.p. 63°-65° C. Elemental analysis: found C, 76.6; H, 6.5; P, 8.2%; C24H25O2P requires: C, 76.6; H, 6.7;P 8.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04036872
Source datasetuspto-grants-1977_07
ORD IDord-8c5d8aed142748ad959f05a6a779aefe
Source noteuspto-grants-1977_07