HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 5-(4-Fluorophenyl)-3-(p-bromomethylphenyl)-1,2,4-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-(4'-Fluorophenyl)-3-(p-tolyl)-1,2,4-thiadiazole | HCID 22611069 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 5-(4-Fluorophenyl)-3-(p-bromomethylphenyl)-1,2,4-thiadiazole | HCID 22611062 | 106.8% |
Reaction Steps
To a solution of 5-(4′-fluorophenyl)-3-(p-tolyl)-1,2,4-thiadiazole (0.16 g, 0.59 mmol) in CCl4 (20 ml) is added NBS (0.11 g, 0.59 mmol) and the mixture is heated to reflux for 36 hours. The mixture is cooled to room temperature and filtered through celite. The mother liquor is concentrated. The residue is taken up in chloroform (30 ml) amd washed with water (30 ml). The organic layer is dried over MgSO4 and concentrated to yield 5-(4′-fluorophenyl)-3-(p-bromomethylphenyl)-1,2,4-thiadiazole, (0.22 g) as crude product which is used as is without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06281217B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-caae91279d384e8a8acde34588ff1039 |
| Source note | uspto-grants-2001_08 |