HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 23298010, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 7-Bromo-2,3-dimethoxy-5-methylquinoxaline | HCID 23298050 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 23298010 | HCID 23298010 | — |
Reaction Steps
15 g (53 mmol) of 7-bromo-5-methyl-2,3-dimethoxy-quinoxaline, 9.9 g (1.05 equiv.) of N-bromosuccinimide and 0.87 g (0.1 equiv.) of azo-isobutyronitrile are dissolved in 100 ml of carbon tetrachloride and the solution is stirred at reflux for 24 hours. The solid is filtered off and the filtrate is diluted with dichloromethane, then washed once with each of water and brine. The organic phase is dried over magnesium sulfate and concentrated by evaporation. The residue is recrystallized from ethyl acetate and hexane. The title compound is obtained in the form of light-orange crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06080743 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-94c68e858ea046f886de8dc83e034cfe |
| Source note | uspto-grants-2000_06 |