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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911494Generated: November 2, 2026

Ethanol → 4-Amino-2-(trifluoromethoxy)phenol

https://huagongshe.com/reaction/1911494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantAmmonia chlorideHCID 20976574—
Reactant4-Nitro-2-(trifluoromethoxy)phenolHCID 70699572—
SolventWaterHCID 962—
Product4-Amino-2-(trifluoromethoxy)phenolHCID 1133300474.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

223 mg (1.0 mmol) of 4-nitro-2-trifluoromethoxyphenol, 224 mg (4.0 mmol) of reduced iron powder, and 321 mg (6.0 mmol) of ammonia chloride were successively added to a mixture of 20 mL of ethanol and 6.0 mL of water under argon atmosphere with mechanical stirring. The mixture was slowly heated to 50° C. and allowed to react at this temperature for 1.5 h until the solution turned brown. The reaction was stopped, naturally cooled, filtered under reduced pressure, and the filter cake was washed with 10 mL of ethyl acetate. 20 mL of water and 20 mL of ethyl acetate were added to the filtrate. The organic layer was isolated, and the water layer was extracted with 20 mL×2 of ethyl acetate. The organic layers were combined, successively washed with 50 mL of water and 50 mL of saturated saline, dried over anh. MgSO4, filtered and concentrated to obtain 144 mg of a dark red solid. Yield 74.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604065B2
Source datasetuspto-grants-2013_12
ORD IDord-da447fb67b624efea2d9a0a037aef0fa
Source noteuspto-grants-2013_12