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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323111Generated: October 27, 2026

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

https://huagongshe.com/reaction/323111

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211373B1
Source datasetuspto-grants-2001_04
ORD IDord-69ca5bf0c43b45a5badc27606023348a
Source noteuspto-grants-2001_04