HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 5-Bromo-4-methoxythiophene-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 15669338 | HCID 15669338 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-4-methoxythiophene-2-sulfonamide | HCID 22019529 | 82.1% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 4-methoxythiophene-2-sulfonamide (240 mg, 1.24 mmol) in CH2Cl2 (40 mL) is added N-bromosuccinimide (287 mg, 1.61 mmol). The reaction mixture is stirred at 0° C. for 7 hr. After 7 hr, the reaction mixture is diluted with CH2Cl2 (150 mL). The organic layer is washed with brine then dried (Na2SO4), filtered and concentrated in vacuo. The crude product is chromatographed on silica gel, eluting with Hex:EtOAc (2:1) to afford the title compound (277 mg, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084170B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-691061cfa6dd4a19863f6daf18e6a0b4 |
| Source note | uspto-grants-2006_08 |