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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612710Generated: November 2, 2026

2-Nitro-4-(trifluoromethyl)phenol → 2-Amino-4-(trifluoromethyl)phenol

https://huagongshe.com/reaction/612710

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitro-4-(trifluoromethyl)phenolHCID 9816—
ReactantSodium HydroxideHCID 14798—
ReactantStannous ChlorideHCID 24479—
SolventEthanolHCID 702—
Product2-Amino-4-(trifluoromethyl)phenolHCID 12024683.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-trifluoromethyl-2-nitrophenol (1.0 g, 4.8 mmol) and tin (II) chloride (5.4 g, 24.2 mmol) in ethanol (150 mL) was heated at 80° C. under argon. After 2 hours, the starting material had disappeared and the solution was allowed to cool down and then poured into ice. The pH was made slightly basic (pH7-8), by addition of solid NaOH, before being extracted with ethyl acetate. The organic phase was washed with brine, dried over MgSO4 and filtered. The solvent was evaporated and chromatography of the resulting solid on silica gel (4% MeOH/CH2Cl2) gave the desired product (708 mg, 83%). 1H NMR (CD3OD): δ6.87 (s, 1H), 6.80 (d, 1H), 6.69 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06005008
Source datasetuspto-grants-1999_12
ORD IDord-51c22c39a1f1419f9b62bc4e6b68ae0d
Source noteuspto-grants-1999_12