HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867019Generated: October 30, 2026
Hydrochloric Acid → (2-Fluorophenyl)(piperidin-4-yl)methanone--hydrogen chloride (1/1)
https://huagongshe.com/reaction/867019
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 13180319 | HCID 13180319 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2-Fluorophenyl)(piperidin-4-yl)methanone--hydrogen chloride (1/1) | HCID 13180313 | — |
Reaction Steps
A solution of 40.5 g of 1-phenoxycarbonyl-4-(2-fluorobenzoyl)piperidine in 500 ml of ethanol and 500 ml of an aqueous 30% potassium hydroxide solution is stirred at a temperature slightly below reflux for 16 hours, allowed to cool to ambient temperature, diluted with water, and the ethanol is partially removed under reduced pressure. The resulting aqueous suspension is extracted with ether, the combined ether extracts are extracted with 1N hydrogen chloride and the aqueous acid solution is basified with an aqueous sodium hydroxide solution. The basic solution is extracted with ether, the combined ether extracts are dried and the ether is removed under reduced pressure leaving a dark oil. The oil is dissolved in a minimum amount of ethanol and ethereal-hydrogen chloride is added dropwise to effect a precipitate. The precipitate is collected by filtration, dried and recrystallized twice from an ethanol-ether mixture to give a white solid, mp 185°-187° C., 4-(2-fluorobenzoyl)piperidine hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04101663 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-65f06ed50f84414b8e821e9b53b4e77b |
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| Source note | uspto-grants-1978_07 |
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