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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971677Generated: October 29, 2026

Hydrogen Peroxide → 3,4-Epoxy-1-(beta,beta,beta-trichloroethoxycarbonyl)-pyrrolidine

https://huagongshe.com/reaction/971677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium Phosphate, DibasicHCID 24203—
ReactantN-(beta,beta,beta-trichloroethoxycarbonyl)-3-pyrrolineHCID 13192204—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3,4-Epoxy-1-(beta,beta,beta-trichloroethoxycarbonyl)-pyrrolidineHCID 13192205—

Reaction Steps

12 ml of 90% strength hydrogen peroxide (0.48 mol) are dissolved in 40 ml of methylene chloride and the solution is treated at 0° with 63.5 ml (0.45 mol) of trifluoroacetic anhydride. After stirring for 15 minutes at 0°, the solution is added dropwise to a suspension, which is kept at 0°, of 196 g of anhydrous disodium hydrogen phosphate in 800 ml of methylene chloride, in which 41.8 g (0.17 mol) of N-(β,β,β-trichloroethoxycarbonyl)-3-pyrroline has been dissolved. Subsequently, the reaction mixture is stirred for 2 hours at room temperature and then stirred into 900 ml of water and the resulting mixture is stirred for a further one hour. The organic phase is separated off and the aqueous phase is extracted by shaking with 3 times 200 ml of methylene chloride; the combined organic phases are washed successively with aqueous sodium chloride solution, aqueous iron-II sulphate solution and then with water, dried over sodium sulphate and evaporated under a water pump vacuum, whereupon 3,4-epoxy-1-(β,β,β-trichloroethoxycarbonyl)-pyrrolidine is obtained in the form of white crystals with a melting point of 52°-55°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04160837
Source datasetuspto-grants-1979_07
ORD IDord-09e0f1670b1544db8092eb0967e91e32
Source noteuspto-grants-1979_07