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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230115Generated: October 31, 2026

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

https://huagongshe.com/reaction/230115

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 numberUS07566717B2
Source datasetuspto-grants-2009_07
ORD IDord-eef53b2d7396407cabf6e83b129ecf40
Source noteuspto-grants-2009_07