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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37372Generated: October 28, 2026

Sodium borohydride → 1-Benzyl-4-(phenylamino)piperidine-4-methanol

https://huagongshe.com/reaction/37372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19935652HCID 19935652—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1-Benzyl-4-(phenylamino)piperidine-4-methanolHCID 301723076%

Reaction Steps

Sodium borohydride (2 g) was added portionwise to a stirred solution of 4-(N-phenylamino)-1-phenylmethyl-piperidine-4-carboxaldehyde (2 g) in methanol at room temperature. After stirring at room temperature for 2 hours the mixture was diluted with water, extracted with chloroform and the combined extracts washed and dried. After removal of the solvent, the crude product was purified by chromatography on silica gel, using chloroform/methanol (38:1) as eluant, to give the title compound (1.53 g) 4-(N-phenylamino)--1-phenylmethyl-4-piperidinylmethanol is then converted to sufentanil following the method described in U.S. Pat. No. 4,179,469 and as illustrated by FIG. 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420280
Source datasetuspto-grants-1995_05
ORD IDord-3f041f1a149f4c3da5afef44e7d0f088
Source noteuspto-grants-1995_05