HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → 2-Methyl-2,3-dihydro-1-benzofuran-7-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 5-Bromo-2-methyl-2,3-dihydro-1-benzofuran-7-sulfonamide | HCID 20222558 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Methyl-2,3-dihydro-1-benzofuran-7-sulfonamide | HCID 20222556 | 79.3% |
Reaction Steps
72.5 g (0.25 mole) of 5-bromo-2,3-dihydro-2-methyl-7-sulfamoylbenzo[b]furan are hydrogenated in the presence of 22.4 g (0.25 mole) of sodium acetate and 7.5 g of 5% palladium on carbon catalyst in 750 ml of methanol. The catalyst is removed, the solvent evaporated, and the residue crystallised from a mixture of water/ethanol, affording 42.3 g (79% of theory) of 2,3-dihydro-2-methyl-7-sulfamoylbenzo[b]furan with a melting point of 174°-177° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04634465 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-4699cda7af36402b85fcc904772761a7 |
| Source note | uspto-grants-1987_01 |