Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169309Generated: November 2, 2026

Sodium borohydride → (1-Phenylcyclopentyl)methanol

https://huagongshe.com/reaction/2169309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-Phenylcyclopentane-1-carbaldehydeHCID 11095124—
SolventMethanolHCID 887—
Product(1-Phenylcyclopentyl)methanolHCID 123544—

Reaction Steps

To a stirred solution of 1-phenyl-cyclopentanecarbaldehyde (277) (11.5 g, 71.82 mmol) in methanol (150 mL) was added NaBH4 at 0° C. portion-wise and the reaction was stirred at room temperature for 2 h. After completion of the reaction, the reaction mixture was quenched with a saturated aqueous solution of ammonium chloride (20 mL). Subsequently, the methanol was removed, the residue diluted with water (100 mL) and extracted with ethyl acetate (3×100 mL) and the separated organic part was dried and concentrated. The crude product was purified by Combi-Flash column (eluted at 5-10% ethyl acetate in hexane) to get (1-phenyl-cyclopentyl)-methanol] (278) (10 g, 79.0%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-fe5ba759481f42868ed98d12c321587e
Source noteuspto-grants-2015_06