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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056106Generated: November 2, 2026

Sodium Thiosulfate → 2-Amino-4-(trifluoromethoxy)phenol

https://huagongshe.com/reaction/2056106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactant2-Nitro-4-(trifluoromethoxy)phenolHCID 2775775—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-Amino-4-(trifluoromethoxy)phenolHCID 273772956.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 2-nitro-4-(trifluoromethoxy)phenol (2 g, 0.0089 mol) in ethanol (50 mL) and water (25 mL) was added sodium thiosulfate (6.2 g, 0.0356 mol) at room temperature. The heterogeneous mixture was stirred at 80° C. under an atmosphere of nitrogen for 1 hour. The reaction mixture was cooled to room temperature, and ethanol was removed under reduced pressure. The aqueous layer was extracted with ethyl acetate (3×70 mL), and the organic layer was washed with brine and dried under sodium sulfate. The solvent was removed under reduced pressure to give yellow solid of 2-amino-4-(trifluoromethoxy)phenol (0.9 g, 0.005 mol). TLC (methanol/dichloromethane=5:95) Rf 0.29 MS: MH+: 194

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332497B2
Source datasetuspto-grants-2008_02
ORD IDord-396109b6c4e849f59544872c39ac9450
Source noteuspto-grants-2008_02