Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(4-Chlorophenyl)-4-hydroxypiperidine | HCID 38282 | — |
| Reactant | HCID 20360374 | HCID 20360374 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | HCID 20360356 | HCID 20360356 | — |
Reaction Steps
A mixture of 10 parts of N-(2-chloroethyl)-α-phenylbenzenemethanamine hydrochloride 7 parts of 4-(4-chlorophenyl)-4-piperidinol, 10.6 parts of sodium carbonate, 0.1 parts of potassium iodide and 80 parts of 4-methyl-2-pentanone is stirred and refluxed overnight. The reaction mixture is taken up in water and the layers are separated. The aqueous phase is extracted with 4-methyl--pentanone. The combined organic phases are washed with water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (96:4 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from a mixture of methylbenzene and 2,2'-oxybispropane. The product is filtered off and dried, yielding 4.5 parts of 4-(4-chlorophenyl)-1-{2-[(diphenylmethyl)amino]ethyl}-4-piperidinol; mp. 113.9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04082755 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-a9a6c932ab984e4883eb8ee48cae4bb4 |
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| Source note | uspto-grants-1978_04 |
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