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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036921Generated: October 30, 2026

HCID 67291102, compound → 2-(4,4-Dimethyl-6-(trifluoromethyl)-1,2,3,4-tetrahydroquinolin-2-yl)aniline

https://huagongshe.com/reaction/1036921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67291102HCID 67291102—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventAmmonium ChlorideHCID 25517—
Product2-(4,4-Dimethyl-6-(trifluoromethyl)-1,2,3,4-tetrahydroquinolin-2-yl)anilineHCID 67289989—

Reaction Steps

To a suspension of 4,4-dimethyl-2-(2-nitrophenyl)-6-(trifluoromethyl)-1,2,3,4-tetrahydroquinoline (2.56 g, 7.3 mmol) in saturated aqueous ammonium chloride (20 mL) and ethanol (30 mL) was added iron powder (1.2 g, 21.0 mmol) at room temperature After addition, the resulting mixture was stirred at reflux under Nitrogen for 3 h. The reaction mixture was cooled to room temperature and filtered through a pad of celite. The solvent of ethanol in filtrate was removed under reduced pressure and the water phase was extracted with ethyl acetate. The combined organic phase was dried, concentrated to give 2-(4,4-dimethyl-6-(trifluoromethyl)-1,2,3,4-tetrahydroquinolin-2-yl)aniline. The product was used in the next step without further purification. LC/MS m/e obsd. (ESI+) [(M+H)+] 321.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546427B2
Source datasetuspto-grants-2013_10
ORD IDord-8ad61d17f5d042288f6a29ed579881dd
Source noteuspto-grants-2013_10