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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709860Generated: November 2, 2026

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

https://huagongshe.com/reaction/1709860

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

A mixture of 93 g of (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 1 hr. The mixture was poured onto ice and the 2 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% yield) 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 numberUS04950674
Source datasetuspto-grants-1990_08
ORD IDord-6318ce07033c4e3faf2d5fb5c990841d
Source noteuspto-grants-1990_08