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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464571Generated: October 25, 2026

Phosgene → (2-Chloroethyl)phosphonic dichloride

https://huagongshe.com/reaction/464571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantPhosphonic dichloride, ethenyl-HCID 74035—
ReactantPoly(vinylphosphonic acid)HCID 168725—
Solvent1,2-DichloroethaneHCID 11—
Product(2-Chloroethyl)phosphonic dichlorideHCID 69645—
ProductPhosphonic dichloride, ethenyl-HCID 74035—

Reaction Steps

298 g of the vinylphosphonic acid derivatives thus prepared are metered into 300 g of vinylphosphonic acid dichloride at 145° C. during the course of 4 hours, whilst stirring, during which time phosgene gas is continuously introduced into the reaction mixture. The reaction mixture is then further phosgenated for 10 hours at this temperature. 1,2-Dichloroethane which is formed distils off during the phosgenation. After the phosgenation has ended, the excess phosgene is stripped off at room temperature in the vacuum from a water jet. The mixture is then distilled at 2 mm Hg with the aid of a column. 430 g of vinylphosphonic acid dichloride and 140 g of 2-chloroethanephosphonic acid dichloride are obtained. The distillation residue is 39 g. 130 g of vinylphosphonic acid dichloride and 140 g of 2-chloroethanephosphonic acid dichloride were thus prepared from 298 g of vinylphosphonic acid derivatives. The 2-chloroethanephosphonic acid dichloride can again be employed as the reaction medium in a second mixture, instead of the vinylphosphonic acid dichloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04548762
Source datasetuspto-grants-1985_10
ORD IDord-25d1c16c6c294e8e9cbd790bf3c62f03
Source noteuspto-grants-1985_10