HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 6-(Bromomethyl)benzo[d]oxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-Methylbenzoxazole | HCID 2724969 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-(Bromomethyl)benzo[d]oxazole | HCID 21985057 | 77.9% |
Reaction Steps
A mixture of 6-methylbenzoxazole (5.0 g; J. T. Gupton, K. F. Correia and B. S. Foster, Synthetic Communications, 1986, 16, 365), N-bromosuccinimide (7.0 g) and azobisisobutyronitrile (0.55 g) in dry chloroform (100 ml) was heated at reflux for 1 hour. The cooled reaction mixture was washed three times with water (40 ml), dried over magnesium sulphate and evaporated. The residual orange coloured viscous solid was triturated twice with pentane (50 ml) affording the title compound (6.20 g) as a buff coloured solid, m.p. 52-56° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06124343 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-8df8eb1fff2e4705a603a381baf6df89 |
| Source note | uspto-grants-2000_09 |