Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926515Generated: October 31, 2026

Acetic Anhydride → 1-Acetyl-4-(4-fluorobenzoyl)piperidine

https://huagongshe.com/reaction/926515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant4-(4-Fluorobenzoyl)piperidineHCID 2724440—
SolventDichloromethaneHCID 6344—
Product1-Acetyl-4-(4-fluorobenzoyl)piperidineHCID 117257—

Reaction Steps

Acetic anhydride (2.32 g, 24.6 mmol) was added dropwise to a cold (0° C.) solution of (4-fluorophenyl)(piperidin-4-yl)methanone (5.00 g, 20.5 mmol) in DCM (33 mL) and triethylamine (10.0 mL, 71.8 mmol). The resulting mixture was removed from the ice bath after 5 minutes and stirred at room temperature for 2 hours. The reaction was then added to a mixture of 1 M aqueous K3PO4 (100 mL), H2O, and DCM. The layers were separated and the aqueous layer again extracted with DCM. The combined organic layers were dried (Na2SO4), filtered, concentrated under reduced pressure and chromatographed (DCM/EtOAc) to provide the title compound as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284308B2
Source datasetuspto-grants-2016_03
ORD IDord-b5c26ba8094a4d36858e5d9c3ad1f340
Source noteuspto-grants-2016_03