HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-[p-Chlorobenzoyl]-1-methylpiperidine → alpha-[4-Chlorophenyl]-1-methyl-4-piperidinemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-[p-Chlorobenzoyl]-1-methylpiperidine | HCID 242680 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | alpha-[4-Chlorophenyl]-1-methyl-4-piperidinemethanol | HCID 541856 | 100.1% |
Reaction Steps
To a solution of 4-chlorophenyl 1-methylpiperidin-4-yl methanone 1.19 g (5 mmol) in 30 ml methanol was added in small portions sodium borohydride 0.378 g (10 mmol). The reaction mixture was stirred at room temperature for two hours, concentrated, added water and extracted with methylene chloride 2×50 ml. The combined organic solution was dried over sodium sulfate and concentrated to give 1.2 g of desired product in 98% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07659395B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-ed72078baf4a44aab07c5473d94b7a8a |
| Source note | uspto-grants-2010_02 |