HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 2-Bromo-4-chloro-6-methoxy-3-methylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Chloro-5-methyl-o-anisidine | HCID 80782 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Bromo-4-chloro-6-methoxy-3-methylaniline | HCID 71427814 | 62% |
Reaction Steps
N-Bromosuccinimid (3.9 g, 22 mmol) was added to 4-chloro-2-methoxy-5-methylanilin (4.04 g, 20 mmol) dissolved in acetonitril (200 ml). The reaction was stirred at r.t. overnight, and the solvent was evaporated. The residue was purified by column chromatography (silica gel, methylene chloride) to yield the title compound (3.1 g, 62%) as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07790733B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-c7aa83a95d964f048c8c3b263b292300 |
| Source note | uspto-grants-2010_09 |