HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-(1-Methoxycarbonylethoxy)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 2-bromopropionate | HCID 95576 | — |
| Reactant | 2-Hydroxybenzene-1-sulfonamide | HCID 637546 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(1-Methoxycarbonylethoxy)benzenesulfonamide | HCID 22152837 | 80.7% |
Reaction Steps
34.6 g of 2-hydroxybenzenesulfonamide and 55.3 g of potassium carbonate are added to 800 ml of acetonitrile. With efficient stirring, 33.4 g of methyl 2-bromopropionate are added dropwise over 10 minutes and the suspension is then heated for 5 hours to 45° C. After the reaction mixture has cooled, the precipitated salts are isolated and the filtrate is concentrated in vacuo. The residue is recrystallised from ethanol, affording 41.8 g of 2-(1-methoxycarbonylethoxy)-benzenesulfonamide with a melting point of 140°-142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04978383 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-efa59f1022474e0f8f171d7ed542b7fc |
| Source note | uspto-grants-1990_12 |