HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464662Generated: October 31, 2026
Hydrogen Bromide → (4-Fluorophenyl)(4-phenyl-4-piperidinyl)methanone hydrobromide hemihydrate
https://huagongshe.com/reaction/464662
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Ethyl 4-(4-fluorobenzoyl)-4-phenylpiperidine-1-carboxylate | HCID 13477817 | — |
| Solvent | Water | HCID 962 | — |
| Product | (4-Fluorophenyl)(4-phenyl-4-piperidinyl)methanone hydrobromide hemihydrate | HCID 70478562 | — |
Reaction Steps
A mixture of 14 parts of ethyl 4-(4-fluorobenzoyl)-4-phenyl-1-piperidinecarboxylate and 150 parts of a hydrobromic acid solution 48% in water was stirred and refluxed for 30 minutes. The reaction mixture was diluted with 100 parts of water and the whole was stirred while the mixture was allowed to cool to room temperature. The precipitated product was filtered off (filtrate I was set aside), washed with methylbenzene and stirred in 2-propanone. It was filtered off again (filtrate II was set aside) and dried, yielding a first fraction of 4.3 parts of (4-fluorophenyl)(4-phenyl-4-piperidinyl)methanone hydrobromide hemihydrate. Filtrates I and II were evaporated and the solid residue was stirred in 4-methyl-2-pentanone. The product was filtered off and dried, yielding a second fraction of 6.2 parts of (4-fluorophenyl) (4-phenyl-4-piperidinyl)methanone hydrobromide hemihydrate; mp. 173.4° C. Total yield: 73%. (intermediate 17).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04548938 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-c96abf8c93464b60a1440b62632c1a8e |
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| Source note | uspto-grants-1985_10 |
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