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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(2-hydroxy-2-phenylethyl)acetamide | HCID 270963 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | n-(2-Oxo-2-phenylethyl)acetamide | HCID 226684 | 53% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06049006 |
|---|
| Source dataset | uspto-grants-2000_04 |
|---|
| ORD ID | ord-94c4313e458c450c83f74169d7548441 |
|---|
| Source note | uspto-grants-2000_04 |
|---|