Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 4'-tert-Butyl-4-chlorobutyrophenone | HCID 2723694 | — |
| Reactant | HCID 12795120 | HCID 12795120 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21568339 | HCID 21568339 | — |
Reaction Steps
A mixture of 11 g (0.035 mole) of α-phenyl-α-(p-chlorophenyl)-4-piperidinemethanol, 12.5 g (0.05 mole) of 4'-tert-butyl-4-chlorobutyrophenone, 10 g of potassium bicarbonate, 0.1 g of potassium iodide, 100 ml of toluene and 10 ml of water is refluxed with stirring for about 93 hours. Upon cooling to room temperature the mixture is filtered and the toluene layer is separated. The aqueous layer is extracted with toluene. The combined organic fractions are washed with water and saturated sodium chloride solution, dried over magnesium sulfate, and filtered. To the filtrate is added an equal volume of ether followed by treatment with ethereal HCl. The resulting precipitate is collected and recrystallized from methanol-butanone to give 4'-tert-butyl-4-[4-[α-hydroxy-α-(p-chlorophenyl)benzyl]-piperidino]butyrophenone hydrochloride, M.P. 238.5°-240°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03931197 |
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| Source dataset | uspto-grants-1976_01 |
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| ORD ID | ord-7308669c48824978b118ea29e628ebca |
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| Source note | uspto-grants-1976_01 |
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