HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 23298034, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 23298052 | HCID 23298052 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 23298034 | HCID 23298034 | — |
Reaction Steps
8.4 g (37.8 mmol) of 2,3-dimethoxy-7-fluoro-5-methylquinoxaline, 7.4 g (41.6 mmol) of N-bromosuccinimide and 0.63 g (0.38 mmol) of azoisobutyronitrile are introduced into 140 ml of carbon tetrachloride and stirred at reflux for 6 hours. The reaction mixture is cooled and concentrated, and the residue is taken up in diethyl ether. The suspension is filtered off and the mother liquor is concentrated again. The remaining crude product is recrystallized from hexane. The title compound is obtained as white crystals of m.p. 122-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06117873 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-0f4c4d7ec5a94caf841a8b08a4322a18 |
| Source note | uspto-grants-2000_09 |