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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Fluorobenzene | HCID 10008 | — |
| Reactant | 1-Acetylpiperidine-4-carbonyl chloride | HCID 100950 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 1-Acetyl-4-(4-fluorobenzoyl)piperidine | HCID 117257 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04950674 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-6318ce07033c4e3faf2d5fb5c990841d |
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| Source note | uspto-grants-1990_08 |
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