HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-Hydroxybenzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-Methoxybenzene-1-sulfonamide | HCID 4739144 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Hydroxybenzene-1-sulfonamide | HCID 637546 | 69.6% |
Reaction Steps
22.2 ml of boron tribromide are added dropwise, under nitrogen and at room temperature, over 15 minutes to a suspension of 39 g of 2-methoxyphenylsulfonamide in 210 ml of dry methylene chloride. The reaction mixture is then stirred for 1 hour at room temperature. After the mixture has been cooled to 0° C., 200 ml of methanol are added over 15 minutes and the clear solution is concentrated. The oily residue is taken up in ethyl acetate and the solution is washed twice with water, dried over sodium sulfate, and evaporated to dryness. The residue is triturated with petroleum ether, affording 25.1 g of 2-hydroxyphenylsulfonamide with a melting point of 136°-138° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04425154 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-63899402aea5488aa23ccb345856c681 |
| Source note | uspto-grants-1984_01 |