HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-[2-(Methanesulfonyloxy)ethyl]benzofurazan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 5-(2-Hydroxyethyl)benzofurazan | HCID 15026086 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-[2-(Methanesulfonyloxy)ethyl]benzofurazan | HCID 15166381 | 96.3% |
Reaction Conditions
| Temperature | -30 °C |
|---|
Reaction Steps
5-(2-Hydroxyethyl)benzofurazan (1.48 g, 9 mmol) was dissolved in dichloromethane (45 ml) and triethylamine (1.88 ml, 1.37 g, 13.5 mmol) was added. The mixture was cooled to -30° C. and methanesulfonyl chloride (0.84 ml, 1.24 g, 10.8 mmol) was added dropwise over 5 min. The mixture was stirred at -30° C. for 15 min. and dichloromethane (100 ml) was added. The mixture was washed with water (100 ml), dried (Na2SO4) and evaporated under reduced pressure to give the benzofurazan as a yellow solid (2.10 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05633247 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-09b8475db80c4c40aa60750fe9e33c66 |
| Source note | uspto-grants-1997_05 |