HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Methyl 3-amino-6-bromo-5-fluoro-2-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 3-amino-5-fluoro-2-methylbenzoate | HCID 53419617 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 3-amino-6-bromo-5-fluoro-2-methylbenzoate | HCID 59145869 | 89.7% |
Reaction Steps
To a solution of methyl 3-amino-5-fluoro-2-methylbenzoate (1.37 g, 7.48 mmol) in acetonitrile (57 mL) was added N-bromosuccinimide (1.01 g, 5.66 mmol) under ice-cooling, and the mixture was stirred for 2 hr. The reaction solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=10/90→30/70) to give the title compound (1.33 g, yield 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08247429B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-dcc2122e14cb48eb99102b147426f582 |
| Source note | uspto-grants-2012_08 |