HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 12804767, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 12804754 | HCID 12804754 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12804767 | HCID 12804767 | — |
Reaction Steps
1.5 g of 1-methyl-4-[α-(2-fluoro-4-methylphenyl)-2-tolyl]-4-piperidinol, Example 4, is treated carefully with 7 ml of benzoyl chloride with stirring and cooling. The reaction mixture is stirred for 16 hours at ambient temperature and then diluted with 15 ml of ether. The resulting precipitate is filtered, washed with ether, converted to the free base which is column chromatographed on an alumina column using ether as the eluant. The free base is converted to its hydrogen chloride salt which is recrystallized from a methanol-acetone-ether mixture to give a white powder, mp 218°-219° C. of 4-benzoyloxy-4-[α-(2-fluoro-4-methylphenyl)-2-tolyl]-1-methylpiperidine hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04311703 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-e0234696d14c4b50bea6842161eeeb5f |
| Source note | uspto-grants-1982_01 |