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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Fluorobenzene | HCID 10008 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 1-Acetyl-3-piperidinecarboxylic acid | HCID 14043896 | — |
| Product | 1-Acetyl-3-(4-fluorobenzoyl)piperidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115750B1 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-93185d6358e24a2fbd191c741a8ee011 |
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| Source note | uspto-grants-2006_10 |
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