Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429182Generated: October 29, 2026

4-Hydroxy-4-phenyl-1-(piperidin-1-yl)butan-1-one → HCID 558699, compound

https://huagongshe.com/reaction/429182

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxy-4-phenyl-1-(piperidin-1-yl)butan-1-oneHCID 18523499—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
ProductHCID 558699HCID 55869992.1%

Reaction Steps

A mixture of 4-hydroxy-4-phenyl-1-piperidine-1-yl-butan-1-one (4.00 g, 16.2 mmol), prepared in the previous step, and pyridinium chlorochromate (5.23 g, 24.3 mmol) in 150 ml of methylene chloride was stirred at room temperature for 2.25 hours. The reaction was poured onto 400 g of silica gel (230-400 mesh) and the material eluted with methylene chloride-ethyl acetate. Isolation of the major component gave 4-oxo-4-phenyl-1-piperidine-1-yl-butan-1-one (3.66 g, 92%) as a green solid. Recrystallization of a portion of this solid from ethyl acetate-hexane gave an analytically pure sample, mp 52-54° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316467B1
Source datasetuspto-grants-2001_11
ORD IDord-2c5fde81b68e4932b71ff056fa2f52a2
Source noteuspto-grants-2001_11