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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979597Generated: November 1, 2026

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

https://huagongshe.com/reaction/1979597

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 containing 31.2 g of pyridine dissolved 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 2.5 liters 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 which shows a pale yellow color and a state of wax. Yield was 88%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04481284
Source datasetuspto-grants-1984_11
ORD IDord-be17f2bc14f74ba881e26b79077e299b
Source noteuspto-grants-1984_11