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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928078Generated: October 30, 2026

Acetyl chloride → 1-{3-[1-(3-Fluorophenyl)methylidene]piperidin-1-yl}ethanone

https://huagongshe.com/reaction/928078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-[1-(3-Fluorophenyl)methylidene]piperidine hydrochlorideHCID 70983891—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-{3-[1-(3-Fluorophenyl)methylidene]piperidin-1-yl}ethanoneHCID 70984588—

Reaction Steps

Acetyl chloride (0.515 mL) was added to a mixture of 3-[1-(3-fluorophenyl)methylidene]-piperidine hydrochloride (Intermediate 226, 1.5 g) and N,N-di-isopropyl-N-ethylamine (2.52 mL) in anhydrous THF (50 mL) at 0° C. under nitrogen. The mixture was allowed to warm to room temperature and was stirred for 2 hours. The mixture was diluted with water (100 mL) and extracted with ether, washed with brine, dried (Na2SO4) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 75-100% to give 1-{3-[1-(3-fluorophenyl)-methylidene]piperidin-1-yl}ethanone (1.38 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290472B2
Source datasetuspto-grants-2016_03
ORD IDord-4354b4a830df48c2854eeaec51d107b0
Source noteuspto-grants-2016_03