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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897910Generated: October 27, 2026

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

https://huagongshe.com/reaction/897910

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 numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-c729e579dfcc42dd94c6bd422027e908
Source noteuspto-grants-2005_07