HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 7-Methylsulfonyloxymethylbenzo-1,2,3-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1,2,3-Benzothiadiazol-7-ylmethanol | HCID 20096433 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Methylsulfonyloxymethylbenzo-1,2,3-thiadiazole | HCID 20096456 | — |
Reaction Steps
To a solution of 3.32 g of 7-hydroxymethylbenzo-1,2,3-thiadiazole, 3.1 ml of triethylamine and 0.2 g of 4-dimethylaminopyridine in 50 ml of methylene chloride there is added dropwise with cooling at -5° to 0° C. a solution of 2.23 g of methanesulfonyl chloride in 15 ml of dichloromethane, and the mixture is stirred for 2 hours at room temperature. The reaction mixture is then treated with ice-water and extracted several times using dichloromethane. The combined extracts are washed with water, dried and evaporated. Chromatographic purification on silica gel (CH2Cl2) gives the title compound as a viscous resin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05260423 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-d3bf367c5b404175b43a123d4f5cba0a |
| Source note | uspto-grants-1993_11 |