HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → (2-Bromo-6-nitro-4-trifluoromethyl-phenyl)-methyl-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Benzenamine, N-methyl-2-nitro-4-(trifluoromethyl)- | HCID 88405 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (2-Bromo-6-nitro-4-trifluoromethyl-phenyl)-methyl-amine | HCID 68878922 | 69% |
Reaction Steps
To a mixture of methyl-(2-nitro-4-trifluoromethyl-phenyl)-amine (16 g) and acetonitrile (200 ml) was added N-bromosuccinimide (15 g) while ice-cooling. The reaction mixture was stirred at room temperature for 5 hours. To the resulting reaction mixture was poured saturated aqueous sodium hydrogen carbonate solution, and then the mixture was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give (2-bromo-6-nitro-4-trifluoromethyl-phenyl)-methyl-amine (15 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120823B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-f4d5370820b64331a0b24e343d18aeb2 |
| Source note | uspto-grants-2015_09 |