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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419431Generated: November 4, 2026

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

https://huagongshe.com/reaction/1419431

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): δ 6.87 (s, 1H), 6.80 (d, 1H), 6.69 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05886044
Source datasetuspto-grants-1999_03
ORD IDord-f5200ea05bc54dbd8c2bf41eebaf0a65
Source noteuspto-grants-1999_03