HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 5-Chloro-2-hydroxybenzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 5-Chloro-2-methoxybenzene-1-sulfonamide | HCID 13210296 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Chloro-2-hydroxybenzene-1-sulfonamide | HCID 13321756 | 66.1% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a suspension of 5-chloro-2-methoxy-benzenesulfonamide (0.52 g, 2.33 mmol) in dichloromethane (25 mL) at −78° C. was added boron tribromide (1M solution in dichloromethane, 3.5 mL, 3.5 mmol). The reaction was stirred at −78° C. for 30 minutes and then warmed to ambient temperature and stirred overnight. The reaction was quenched with water (0.30 mL) and the precipitate formed was removed by filtration. The filtrate was concentrated in vacuo and the crude product was purified by chromatography on silica gel to give the title compound (0.32 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07098212B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-b01bc6866af44416bdc86c9e87868d5a |
| Source note | uspto-grants-2006_08 |