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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627496Generated: October 25, 2026

Acetic Anhydride → 1-Acetyl-4-benzoylpiperidine

https://huagongshe.com/reaction/627496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
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, Apollo Scientific) in DCM (13.2 mL) and TEA (1.10 mL, 7.90 mmol) was treated with Ac2O (0.373 mL, 3.95 mmol) dropwise over 1 min on 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 partitioned with 1 M HCl (1×8 mL) and 1 M 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 numberUS09309222B2
Source datasetuspto-grants-2016_04
ORD IDord-7e76c6bd2a5040c4997c089712112ea1
Source noteuspto-grants-2016_04