Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004484Generated: October 30, 2026

N-(2-hydroxy-2-phenylethyl)acetamide → n-(2-Oxo-2-phenylethyl)acetamide

https://huagongshe.com/reaction/1004484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-hydroxy-2-phenylethyl)acetamideHCID 270963—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Productn-(2-Oxo-2-phenylethyl)acetamideHCID 22668453%

Reaction Steps

A mixture of N-(2-hydroxy-2-phenyl-ethyl)-acetamide (7.68 g, 43 mmol), prepared in the previous step, and pyridinium chlorochromate (14.0 g, 65 mmol) in 800 ml of methylene chloride was stirred at room temperature for 5 hours. The organic phase was decanted from a black oily residue in the flask. This black residue was triturated with methylene chloride and then with 10% methanol-methylene chloride. The organic phases were concentrated under reduced pressure and the residue chromatographed on 400 g of silica gel (230-400 mesh) using ethyl acetate-methylene chloride as the eluent. Isolation of the desired component gave N-(2-oxo-2-phenyl-ethyl)-acetamide (4.0 g, 53%) as a white solid. The material was used in the following reaction without additional purification, MS m/e (M+H)+ 178.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06049006
Source datasetuspto-grants-2000_04
ORD IDord-94c4313e458c450c83f74169d7548441
Source noteuspto-grants-2000_04