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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242912Generated: November 1, 2026

Fluorobenzene → 1-Acetyl-3-(4-fluorobenzoyl)piperidine

https://huagongshe.com/reaction/1242912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFluorobenzeneHCID 10008—
ReactantThionyl ChlorideHCID 24386—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant1-Acetyl-3-piperidinecarboxylic acidHCID 14043896—
Product1-Acetyl-3-(4-fluorobenzoyl)piperidineHCID 21939813—

Reaction Steps

Thionyl chloride (2.12 ml, 32.1 mmol) was added to fluorobenzene solution (20 ml) of 1-acetyl-3-piperidinecarboxylic acid (5.00 g, 29.2 mmol) under ice-cooling, which was stirred at room temperature for 30 minutes. Aluminum chloride (9.74 g, 73.0 mmol) was added to the solution, which was stirred at 90° C. for 1 hour. The reaction mixture was poured in ice, and extraction was conducted using ethyl acetate. The extract was washed with saturated aqueous sodium chloride solution, saturated sodium hydrogencarbonate solution, and again saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and then the solvent was distilled out under reduced pressure. The resulting oily substance was purified by silica gel column chromatography (development solvent; hexane:ethyl acetate=1:1), to give (1-acetyl-3-piperidinyl)(4-fluorophenyl)methanone (4.93 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115750B1
Source datasetuspto-grants-2006_10
ORD IDord-93185d6358e24a2fbd191c741a8ee011
Source noteuspto-grants-2006_10