Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077694Generated: October 30, 2026

Ethyl chloroformate → HCID 178476786, compound

https://huagongshe.com/reaction/1077694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantEthyl diethoxymethyl(benzyl)phosphinateHCID 9994134—
SolventHydrochloric AcidHCID 313—
SolventDichloromethaneHCID 6344—
ProductHCID 178476786HCID 178476786—

Reaction Steps

A suspension of 128 g of diethoxymethyl(benzyl)phosphinic acid ethyl ester in 400 ml of hydrochloric acid is heated under reflux for 20 hours, cooled to room temperature, washed with diethyl ether/hexane (1:1) and concentrated to dryness by evaporation. The residue is taken up in dichloromethane, dried over sodium sulfate and again concentrated by evaporation. The viscous benzylphosphinic acid that remains is then dried under a high vacuum. 13.34 g of benzylphosphinic acid are dissolved in 150 ml of dichloromethane, the solution is cooled to 5°, and 8.64 g of triethylamine are added dropwise. An exothermic reaction takes place. The mixture is cooled to 5° again, and 9.3 g of chloroformic acid ethyl ester are added dropwise within a period of 30 minutes. A precipitate forms in an exothermic reaction with the evolution of gas. The mixture is allowed to warm to room temperature and is then stirred at room temperature for 3 hours, taken up in dichloromethane and washed with water, and the organic solvent is removed. The crude product is distilled under a high vacuum, yielding benzylphosphinic acid ethyl ester having a boiling point of 96°100° (5×10-6 bar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05545631
Source datasetuspto-grants-1996_08
ORD IDord-5eedf202f3634732a5a951eb363fc55a
Source noteuspto-grants-1996_08