HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-(4-Aminobenzoyl)-4-[(4-fluorophenyl)hydroxymethyl]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(4-Aminobenzoyl)-4-(4-fluorobenzoyl)piperidine | HCID 13603966 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(4-Aminobenzoyl)-4-[(4-fluorophenyl)hydroxymethyl]piperidine | HCID 13825043 | 99.4% |
Reaction Steps
Sodium borohydride (0.058 g) was added to a solution of 1-(4-aminobenzoyl)-4-(4-fluorobenzoyl)piperidine (1.0 g) in methanol (80 ml) and the mixture was stirred at room temperature for 2 hours. Additional sodium borohydride (0.050 g) was added. After being stirred at the same temperature for 1.5 hours, the resultant mixture was concentrated in vacuo. The residue was diluted with water and extracted twice with methylene chloride. The extracts were combined, washed with brine, dried over magnesium sulfate, and concentrated to dryness in vacuo. The powdery residue was washed with diisopropyl ether to give 1-(4-aminobenzoyl)-4-[(4-fluorophenyl)hydroxymethyl]piperidine (1.00 g) as pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04735952 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-a394553276f946d88c4b85415d94a60f |
| Source note | uspto-grants-1988_04 |