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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062581Generated: October 26, 2026

Ethanol → 2-Phenyl-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/1062581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2-PhenylquinolineHCID 71545—
ReactantSodiumHCID 5360545—
SolventWaterHCID 962—
Product2-Phenyl-1,2,3,4-tetrahydroquinolineHCID 10752915—

Reaction Steps

In Scheme A, step 2, the 2-phenyl-1,2,3,4-tetrahydroquinoline of formula (3) is prepared by reducing 2-phenylquinoline of formula (2). For example, 2-phenylquinoline of formula (2) is dissolved in a suitable alcoholic solvent, such as absolute ethanol. Sodium metal is then added and the reaction is allowed to cool to room temperature. The reaction mixture may then be diluted with water and extracted with a suitable organic solvent, such as methylene chloride, ethyl acetate, or chloroform. The combined extracts may then be washed with water and brine, the organic layer is separated and dried and the solvent is evaporated in vacuo to provide the 2-phenyl-1,2,3,4-tetrahydroquinoline of formula (3) which may be used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06962928B2
Source datasetuspto-grants-2005_11
ORD IDord-209114e7ea504d76ac9ea7df8e82e714
Source noteuspto-grants-2005_11