Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271093Generated: November 2, 2026

m-Chloroperbenzoic acid → N-(4-methoxyphenyl)-2-oxiran-2-ylacetamide

https://huagongshe.com/reaction/1271093

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantN-(4-methoxyphenyl)but-3-enamideHCID 18452750—
SolventDichloromethaneHCID 6344—
ProductN-(4-methoxyphenyl)-2-oxiran-2-ylacetamideHCID 58844915—

Reaction Steps

The solution of N-(4-methoxyphenyl)but-3-enamide (9) from the previous reaction was treated with m-chloroperbenzoic acid (2 eq.) and stirred at room temperature for 18 hours. The reaction mixture was diluted with dichloromethane, and washed with 1N sodium hydroxide. The organic phase was separated, dried over magnesium sulfate, filtered, and the filtrate evaporated under reduced pressure to give crude N-(4-methoxyphenyl)-2-oxiran-2-ylacetamide, a compound of formula (10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205303B2
Source datasetuspto-grants-2007_04
ORD IDord-d46fb5af2e40471295de51925e8c9db5
Source noteuspto-grants-2007_04