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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928807Generated: October 26, 2026

Acetic Anhydride → 1-Acetyl-4-benzoylpiperidine

https://huagongshe.com/reaction/928807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant4-Benzoylpiperidine hydrochlorideHCID 2724437—
SolventDichloromethaneHCID 6344—
Product1-Acetyl-4-benzoylpiperidineHCID 2740714—

Reaction Steps

A mixture of phenyl(piperidin-4-yl)methanone hydrochloride (743 mg, 3.29 mmol) in dichloromethane (13.2 mL) and triethylamine (1.10 mL, 7.90 mmol) was treated with Ac2O (0.373 mL, 3.95 mmol) dropwise over 1 minute in an ice bath under argon, and the resulting translucent mixture was immediately removed from the ice bath and stirred at room temperature overnight. The reaction was then extracted with 1 M aqueous HCl (1×8 mL) and 1 M aqueous NaOH (1×8 mL), and the organic layer was dried (Na2SO4), filtered, and concentrated to provide the title compound as a translucent beige oil that crystallized upon standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290476B2
Source datasetuspto-grants-2016_03
ORD IDord-00ed909a173546ab896e4a7a3f3b58d3
Source noteuspto-grants-2016_03