Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446882Generated: October 31, 2026

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

https://huagongshe.com/reaction/1446882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitro-4-(trifluoromethyl)phenolHCID 9816—
ReactantSodium DithioniteHCID 24489—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-Amino-4-(trifluoromethyl)phenolHCID 12024639.9%

Reaction Conditions

Temperature55 °C

Reaction Steps

Sodium dithionite (97.0 g, 0.5 mole) was added in portions over a period of 6 hours to a solution of 2-nitro-4-trifluoromethylphenol (31 g, 0.15 mole) in a mixture of ethanol (120 ml) and water (90 ml), the solution being heated, with stirring, at a temperature of 55° C. during the addition. The mixture was filtered, the filtrate retained, and the collected solid was triturated with ethanol and refiltered. The solvent was removed from the combined filtrates by distillation under reduced pressure to give a yellow solid. The solid was dissolved in water, the aqueous solution extracted with diethyl ether (4×100 ml) and the combined ethereal phases were washed with brine. The ethereal phase was dried over anhydrous magnesium sulfate and the solvent evaporated to give a yellow solid which was recrystallised from petroleum ether (700 ml, bp 100°-120° C.) to give the title compound as a pale yellow solid (10.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04314065
Source datasetuspto-grants-1982_02
ORD IDord-6334f43f584f463aa5a189d3bf5ff654
Source noteuspto-grants-1982_02