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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800664Generated: October 30, 2026

HCID 531812, compound → N-(3-aminophenyl)-3-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/1800664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 531812HCID 531812—
SolventTetrahydrofuranHCID 8028—
ProductN-(3-aminophenyl)-3-(trifluoromethyl)benzamideHCID 2011751966%

Reaction Steps

To a solution of N-(3-nitrophenyl)-3-(trifluoromethyl)benzamide (30.0 g, 96.7 mmol) in tetrahydrofuran (300 mL) was slowly added with heating under reflux aqueous sodium hydrosulfite (97.8 g, 562 mmol) solution (500 mL), and the obtained two-layer solution was vigorously stirred with heating under reflux for 2 days. After cooling the reaction solution to room temperature, the aqueous layer was separated and extracted with ethyl acetate (150 mL×2). The organic layer separated earlier was diluted with ethyl acetate (350 mL), and washed with saturated aqueous sodium hydrogen carbonate solution (150 mL×2) and saturated brine (100 mL). The collected organic layer was washed with saturated aqueous sodium hydrogen carbonate solution (150 mL×2) and saturated brine (150 mL), and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give the title compound (17.8 g, 66%) as a pale-brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344135B2
Source datasetuspto-grants-2013_01
ORD IDord-cda861dc104547c4b5835c20e048ee9e
Source noteuspto-grants-2013_01