Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648509Generated: October 27, 2026

Sodium borohydride → 1-(4-Aminobenzoyl)-4-[(4-fluorophenyl)hydroxymethyl]piperidine

https://huagongshe.com/reaction/648509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(4-Aminobenzoyl)-4-(4-fluorobenzoyl)piperidineHCID 13603966—
SolventMethanolHCID 887—
Product1-(4-Aminobenzoyl)-4-[(4-fluorophenyl)hydroxymethyl]piperidineHCID 1382504399.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04735952
Source datasetuspto-grants-1988_04
ORD IDord-a394553276f946d88c4b85415d94a60f
Source noteuspto-grants-1988_04