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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476930Generated: October 25, 2026

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

https://huagongshe.com/reaction/476930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFluorobenzeneHCID 10008—
Reactant1-Acetylpiperidine-4-carbonyl chlorideHCID 100950—
ReactantAluminum(III) ChlorideHCID 6451240—
Product1-Acetyl-4-(4-fluorobenzoyl)piperidineHCID 11725780%

Reaction Steps

The title compound was prepared as disclosed in U.S. Pat. No. 3,576,810 as follows: A mixture of 93 g (0.7 mole) of aluminum chloride in 150 ml of fluorobenzene was stirred while 70 g (0.37 mole) of 1-acetylisonipecotic acid chloride was added in small portions. After the addition was complete, the mixture was refluxed for one hour. The mixture was poured onto ice and the two resulting layers were separated. The aqueous layer was extracted twice with chloroform and the chloroform extracts were added to the fluorobenzene which was separated previously. The organic solution was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated and 73.7 g (80%) of 1-acetyl-4-(p-fluorobenzoyl)-piperidine was obtained as a crystalline residue. Recrystallization from ligroin-isopropyl ether gave a white crystalline product melting at 75°-78° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886794
Source datasetuspto-grants-1989_12
ORD IDord-79ff20058e874daeb6a8df84bce5fc68
Source noteuspto-grants-1989_12