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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980340Generated: October 29, 2026

Pyridine → 2-{[3-(2-Chloroethanesulfonyl)propanoyl]oxy}ethyl prop-2-enoate

https://huagongshe.com/reaction/1980340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloroformHCID 6212—
Reactant2-Hydroxyethyl acrylateHCID 13165—
Reactant3-(2-Chloroethanesulfonyl)propanoyl chlorideHCID 13668397—
SolventTetrahydrofuranHCID 8028—
Product2-{[3-(2-Chloroethanesulfonyl)propanoyl]oxy}ethyl prop-2-enoateHCID 1366839888.6%

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of 600 ml of tetrahydrofuran, 45.8 g of hydroxyethyl acrylate, and 72 g of 3-(2-chloroethylsulfonyl)propionic acid chloride was placed in a reactor, and while maintaining the temperature at 5° C. or lower by cooling by ice water, a solution of 31.2 g of pyridine in 100 ml of tetrahydrofuran was added dropwise thereto over a period of 1.75 hours. The resulting mixture was further stirred for 2 hours at room temperature. At the end of the time, the reaction mixture was poured into 2,500 ml of ice water, and extraction was performed four times with 300 ml of chloroform. The organic layer thus extracted was dried over sodium sulfate and concentrated to provide 87 g of 2-[3-(chloroethylsulfonyl)propionyloxy]ethyl acrylate. Yield was 88%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04508818
Source datasetuspto-grants-1985_04
ORD IDord-416336a7c3b14036936634d255b022c5
Source noteuspto-grants-1985_04