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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827944Generated: October 27, 2026

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

https://huagongshe.com/reaction/1827944

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 numberUS07056931B2
Source datasetuspto-grants-2006_06
ORD IDord-4c618bcdc1b04c0690100d32180e82aa
Source noteuspto-grants-2006_06