HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-Bromo-2-chloro-6-(trifluoromethyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Chloro-6-(trifluoromethyl)aniline | HCID 2756384 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Bromo-2-chloro-6-(trifluoromethyl)aniline | HCID 16217937 | — |
Reaction Steps
N-bromosuccinimide (910 mg, 5.1 mmol) was added at room temperature to a solution of 2-chloro-6-(trifluoromethyl)aniline (1.0 g, 5.1 mmol) and acetic acid (3 mL) in acetonitrile (10 mL). The mixture was stirred at reflux to 18 h. The reaction mixture was then filtered through celite and concentrated to give the title compound, which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08993593B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-e86951ee787845a19050816024630467 |
| Source note | uspto-grants-2015_03 |