HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N-(3-(trifluoromethyl)benzyl)-2-(2-aminophenyl)isonicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N-(3-(trifluoromethyl)benzyl)-2-(2-nitrophenyl)isonicotinamide | HCID 66586876 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | N-(3-(trifluoromethyl)benzyl)-2-(2-aminophenyl)isonicotinamide | HCID 66588070 | 80.5% |
Reaction Steps
Into a 100-mL round bottom flask, was placed a solution of N-(3-(trifluoromethyl)benzyl)-2-(2-nitrophenyl)isonicotinamide (350 mg, 0.87 mmol, 1.00 equiv) in ethanol/H2O (1/1) (30 mL), iron (489 mg, 8.73 mmol, 10.00 equiv), and acetic acid (0.1 mL). The resulting solution was heated to reflux for 0.5 h. The solids were filtered out. The resulting solution was extracted with of ethyl acetate and the organic layers combined and dried over magnesium sulfate. The solids were filtered out. The resulting mixture was concentrated under vacuum. The product was obtained as 260 mg (80%) of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08916569B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-e91c4181b45241bc8e43ff65bab74e3c |
| Source note | uspto-grants-2014_12 |