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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422210Generated: October 31, 2026

N-bromobutanimide → HCID 23298010, compound

https://huagongshe.com/reaction/1422210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant7-Bromo-2,3-dimethoxy-5-methylquinoxalineHCID 23298050—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 23298010HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080743
Source datasetuspto-grants-2000_06
ORD IDord-94c68e858ea046f886de8dc83e034cfe
Source noteuspto-grants-2000_06