HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[4-bromo-3-(trifluoromethyl)phenyl]-2-nitrobenzamide → 2-Amino-N-(4-bromo-3-trifluoromethylphenyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[4-bromo-3-(trifluoromethyl)phenyl]-2-nitrobenzamide | HCID 1300995 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Amino-N-(4-bromo-3-trifluoromethylphenyl)benzamide | HCID 11268358 | — |
Reaction Steps
A solution of 2-nitro-N-(4-bromo-3-trifluoromethylphenyl)benzamide (intermediate 1a; 32 g, 82 mmol) in methanol (1000 mL) is hydrogenated at atmospheric pressure over Raney nickel (6 g) at 21° C. The calculated amount of hydrogen is taken up after 7 hours. The mixture is filtered and the solvent is evaporated under reduced pressure to yield the crude product which is purified by recrystallisation from diethylether-hexane to give the title compound as a colourless crystalline solid, m.p. 142-144° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07482369B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-36a9f3960d204e4dbee3f83f68db5887 |
| Source note | uspto-grants-2009_01 |