HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 5-Bromomethyl-4-(4-chlorophenyl)-2-methyloxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Oxazole, 4-(4-chlorophenyl)-2,5-dimethyl- | HCID 11160071 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 5-Bromomethyl-4-(4-chlorophenyl)-2-methyloxazole | HCID 13293293 | — |
Reaction Steps
A solution of 4-(4-chlorophenyl)-2,5-dimethyloxazole (6.21 g), N-bromosuccinimide (5.34 g) and azobisisobutyronitrile (0.25 g) in carbon tetrachloride (90 ml) was refluxed with stirring for 15 minutes, then washed with water, saturated aqueous sodium hydrogen carbonate and water in that order, and dried over anhydrous magnesium sulfate. The solvent was then distilled off and the residue was crystallized from cold ethanol to give 5-bromomethyl-4-(4-chlorophenyl)-2-methyloxazole, yield 6.73 g (78.4%). Recrystallization from ethanol gave needles, melting at 75°-76° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04596816 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-39e7788ed2e845adb0303efd9a11125e |
| Source note | uspto-grants-1986_06 |