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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597371Generated: November 4, 2026

1-(2-Phenylquinolin-4-yl)ethanone → 1-(2-Phenylquinolin-4-yl)-ethanol

https://huagongshe.com/reaction/1597371

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Phenylquinolin-4-yl)ethanoneHCID 344158—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product1-(2-Phenylquinolin-4-yl)-ethanolHCID 2349916662%

Reaction Steps

To 1-(2-phenylquinolin-4-yl)-ethanone (0.233 g, 0.943 mmol) in 5 ml methanol, at room temperature sodium borohydride (0.036 g, 0.943 mmol) was added and the solution stirred for 30 minutes. The reaction mixture was concentrated and partitioned between EtOAc (10 ml) and water (5 ml). The organic layer was dried over sodium sulfate, filtered, concentrated and column purified (hexane:EtOAc; 3.5:1.5) to give 0.145 g (62%) of the product as a syrup which was used as such for the subsequent step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294566B1
Source datasetuspto-grants-2001_09
ORD IDord-09b020983e8b4b53a304e61dd7a7a5a8
Source noteuspto-grants-2001_09