HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267973Generated: October 26, 2026
Potassium Iodide → 4'-Fluoro-5-[4-(alpha-hydroxy-alpha-phenylbenzyl)piperidino]valerophenone hydrochloride
https://huagongshe.com/reaction/267973
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Azacyclonol | HCID 15723 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 5-Chloro-1-(4-fluorophenyl)-1-oxopentane | HCID 12649794 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4'-Fluoro-5-[4-(alpha-hydroxy-alpha-phenylbenzyl)piperidino]valerophenone hydrochloride | HCID 21552952 | — |
Reaction Steps
A mixture of 19.3 g (0.07 mole) of α,α -diphenyl-4-piperidinemethanol, 17.1 g (0.08 mole) of 5-chloro-4'-fluorovalerophenone, 20.0 g (0.2 mole) of potassium bicarbonate, and 0.1 g of potassium iodide in 250 ml of toluene and 35 ml of water is stirred on a steam bath for 70 hours. The organic layer is separated and combined with two 50 ml toluene extracts of the aqueous layer. The combined organic material is washed with water and saturated sodium chloride solution, dried over magnesium sulfate and filtered. The filtrate is diluted with about 200 ml of ether then made acidic with ethereal HCl. The resulting precipitate is recrystallized from methanol-butanone to give 4'-fluoro-5-[4-(α-hydroxy-α-phenylbenzyl)piperidino]valerophenone hydrochloride, M.P. 177°-179°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03946022 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-e7775154740c442a8bdbdf18ccfcf47a |
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| Source note | uspto-grants-1976_03 |
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