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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836302Generated: October 31, 2026

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

https://huagongshe.com/reaction/1836302

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 numberUS06777426B2
Source datasetuspto-grants-2004_08
ORD IDord-a07aadd77aee494787e2508d6788ab86
Source noteuspto-grants-2004_08