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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382011Generated: October 28, 2026

Ethanol → 4-(Trifluoromethyl)aniline

https://huagongshe.com/reaction/1382011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium BicarbonateHCID 516892—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
Reactant4-Triethylsiloxy-4-trifluoromethyl-2,5-cyclohexadien-1-oneHCID 14343494—
SolventWaterHCID 962—
Product4-(Trifluoromethyl)anilineHCID 996473%

Reaction Steps

A mixture of 400 mg (1.4 mmol) of 4-triethylsiloxy-4-trifluoromethyl-2,5-cyclohexadien-1-one, 572 mg (4.2 mmol) of ethyl glycinate hydrochloride, 298 mg (3.6 mmol) of sodium bicarbonate, and 10 mL of 95% ethanol was heated to reflux for 6 hours, allowed to cool to room temperature, and poured into 25 mL of water. The resulting aqueous mixture was extracted with three 10 mL portions of dichloromethane. The organic layers were combined and extracted with six 5 mL portions of 1N HCl. Combination of the aqueous layers and treatment with solid sodium bicarbonate until neutral to pH paper gave a cloudy mixture that was extracted with three 10 mL portions of dichloromethane. The organic layers were combined, dried (MgSO4), and stripped to give a residue which was purified by PTLC (one 2 mm silica gel plate eluted with dichloromethane), affording 160 mg (73% yield) of 4-trifluoromethylaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04804773
Source datasetuspto-grants-1989_02
ORD IDord-a4247fdbb2814206b521dd5ac6261404
Source noteuspto-grants-1989_02