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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346140Generated: October 29, 2026

Triethylamine → 7-cyano-1-phenoxycarbonyloxy-6-trifluoromethylquinoxaline-2,3-(1H,4H)-dione

https://huagongshe.com/reaction/346140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
Reactant7-cyano-1-hydroxy-6-trifluoromethylquinoxaline-2,3(1H,4H)-dioneHCID 19990467—
SolventTetrahydrofuranHCID 8028—
Product7-cyano-1-phenoxycarbonyloxy-6-trifluoromethylquinoxaline-2,3-(1H,4H)-dioneHCID 1999046683%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 0.4 g (1.48 mmol) 7-cyano-1-hydroxy-6-trifluoromethylquinoxaline -2,3(1H,4H)-dione in 50 ml dry tetrahydrofuran was added 0.225 ml (1.63 mmol) dry triethylamine and 0.2 ml (1.58 mmol) phenyl chloroformate. The mixture was stirred at 25° C. for 30 min., and then filtered and evaporated in vacuo. The residue was stirred with ether to give 0.48 g (83%) of 7-cyano-1-phenoxycarbonyloxy-6-trifluoromethylquinoxaline-2,3-(1H,4H)-dione. M.p. 190° C. decomp. 1H-NMR (DMSO-d6): 8.43 (1H,s), 7.63 (1H, s), 7.3 (5H, broad s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05061706
Source datasetuspto-grants-1991_10
ORD IDord-fb0a15971e8e430dad4603c3a94073fb
Source noteuspto-grants-1991_10