HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 4-(2-Bromomethyl-phenyl)-[1,2,3]thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-o-Tolyl-[1,2,3]thiadiazole | HCID 11275338 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(2-Bromomethyl-phenyl)-[1,2,3]thiadiazole | HCID 21866243 | — |
Reaction Steps
A solution of 4-o-tolyl-[1,2,3]thiadiazole (100 mg, 0.57 mmol), N-bromosuccinimide (100 mg, 0.57 mmol) and 2,2′-azobisisobutyronitrile (9.4 mg, 0.057 mmol) in chloroform (10 ml) was heated at reflux temperature for ˜18 h. Additional chloroform was added and the mixture was washed with water, 5% sodium thiosulfate solution and brine. Drying and solvent evaporation gave 4-(2-bromomethyl-phenyl)-[1,2,3]thiadiazole; 1H NMR (CDCl3, 300 MHz) δ 8.87 (s, 1H), 7.67–7.39 (m, 4H), 4.71 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07026324B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-2aedc395aaae42a5b026de86395c53b1 |
| Source note | uspto-grants-2006_04 |