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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701994Generated: October 31, 2026

Acetic Anhydride → n-(2-Oxo-2-phenylethyl)acetamide

https://huagongshe.com/reaction/1701994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantPhenacylamineHCID 11952—
Productn-(2-Oxo-2-phenylethyl)acetamideHCID 226684—

Reaction Steps

About 200 grams of 2-aminoacetophenone were added to about 350 ml. of acetic anhydride at 0° C. After warming to ambient temperature, the reaction mixture was stirred 4 hours and, upon addition of ice water, a precipitate formed which was filtered and washed with water. The precipitate was suspended in ether and washed separately with 1 l. each of 1 N sodium hydroxide, water, 1 N hydrochloric acid, and again with 1 N sodium hydroxide. The ether suspension was dried with sodium sulfate, filtered, and concentrated. Ligroin was added and the desired product was collected by filtration. The identity of the final product was confirmed by NMR analysis; yield 215 grams, m.p. 69° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04379929
Source datasetuspto-grants-1983_04
ORD IDord-7389caec4166419fadaa4bef6c7d2dda
Source noteuspto-grants-1983_04