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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 531812 | HCID 531812 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(3-aminophenyl)-3-(trifluoromethyl)benzamide | HCID 20117519 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08344135B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-cda861dc104547c4b5835c20e048ee9e |
|---|
| Source note | uspto-grants-2013_01 |
|---|