Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275996Generated: October 26, 2026

Acetic Acid → 2',5'-Dimethyl-4'-oxiranylacetanilide

https://huagongshe.com/reaction/275996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant4'-(2-Bromoacetyl)-2',5'-dimethylacetanilideHCID 22169659—
SolventEthanolHCID 702—
Product2',5'-Dimethyl-4'-oxiranylacetanilideHCID 1831676952.1%

Reaction Steps

To a stirred solution of 4′-(2-bromoacetyl)-2′,5′-dimethylacetanilide (4.57 g) in ethanol (80 ml) was added sodium borohydride (608 mg) under ice-cooling, and the mixture was stirred for 1 hour. Acetic acid (3.7 ml) and water (200 ml) were added to the reaction mixture, and the resulting mixture was extracted with ethyl acetate. The extract was washed with water and brine, and dried over anhydrous magnesium sulfate, and the solvent was removed in vacuo. The residue was dissolved in tetrahydrofuran (80 ml), and 5N aqueous sodium hydroxide solution (6.4 ml) was added to the solution under ice-cooling with stirring. The mixture was stirred for 30 minutes at room temperature, water was added to the reaction mixture, and the resulting mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate, and the solvent was removed in vacuo. To the residue was added diethyl ether, and collection of the insoluble material by filtration gave 2′,5′-dimethyl-4′-oxiranylacetanilide (1.72 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353025B1
Source datasetuspto-grants-2002_03
ORD IDord-791e10e64421463a981458982202e6ee
Source noteuspto-grants-2002_03