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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346169Generated: October 30, 2026

Cyclohexyl bromide → HCID 19990417, compound

https://huagongshe.com/reaction/346169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl bromideHCID 7960—
ReactantTriethylamineHCID 8471—
Reactant7-cyano-1-hydroxy-6-trifluoromethylquinoxaline-2,3(1H,4H)-dioneHCID 19990467—
SolventEthanolHCID 702—
ProductHCID 19990417HCID 19990417—

Reaction Steps

To a solution of 0.3 g (1.1 mmol) 7-cyano-1-hydroxy-6-trifluoromethylquinoxaline -2,3(1H,4H)-dione in 30 ml ethanol was added 0.7 ml triethylamine and 1.5 ml (12 mmol) cyclohexylbromide. The reaction mixture was refluxed for 7 days and then evaporated in vacuo. The residue was stirred with water to give a precipitate (0.25 g. Recrystallization (dimethylformamide-water) gave 0.17 g (44%) of 7-cyano-1-cyclohexyloxy-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione). M.p. 259° C. decomp. 1H-NMR (DMSO-d6): 8.0 (1H, s), 7.6 (1H, s), 4.3 (1H, m), 1.4 (8H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05061706
Source datasetuspto-grants-1991_10
ORD IDord-e6d29003c44d4356a642122cf4c5fa97
Source noteuspto-grants-1991_10