HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → (5-Chloro-2-hydroxyphenyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | (5-Chloro-2-methoxyphenyl)methanesulfonamide | HCID 21973342 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | (5-Chloro-2-hydroxyphenyl)methanesulfonamide | HCID 21973532 | 86.8% |
Reaction Steps
To a suspension of (5-chloro-2-methoxy-phenyl)-methanesulfonamide (0.03 g, 0.13 mmol) in dichloroethane (1.5 mL) was added boron tribromide solution (1M in dichloromethane, 0.26 mL, 0.26 mmol). The reaction was stirred for one hour at ambient temperature. The reaction was quenched with water, saturated with sodium chloride and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered and concentrated to give the title compound (0.025 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07098212B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-b4060db022494b248124cc4b060088c2 |
| Source note | uspto-grants-2006_08 |