Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758181Generated: October 26, 2026

Dimethylformamide → 6-pentafluoroethyl-2(1H), 3(4H)-quinoxalinedione

https://huagongshe.com/reaction/1758181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2,3-DihydroxyquinoxalineHCID 27491—
ReactantPentafluoroethylphenyliodonium trifluoromethanesulfonateHCID 11488264—
SolventEthyl AcetateHCID 8857—
Product6-pentafluoroethyl-2(1H), 3(4H)-quinoxalinedioneHCID 128719856%

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of 0.5 g of 2(1H), 3(4H)-quinoxalinedione, 1.60 g of pentafluoroethylphenyliodonium trifluoromethanesulfonate and 10 ml of dimethylformamide was stirred overnight on an oil bath at 45° C. Ethyl acetate was then added to the reaction mixture and the unreacted 2(1H), 3(4H)-quinoxalinedione was removed by filtration (recovery of the starting material: 0.13 g). Water was added to the filtrate and, after rendering the mixture neutral, the mixture was extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate, and the solvent was distilled off. A small amount of methylene chloride was added to the residue and the precipitated crystals were collected by filtration to obtain 0.05 g of 6-pentafluoroethyl-2(1H), 3(4H)-quinoxalinedione as colorless crystals. Yield 6% (conversion yield, 8%). Melting Point (after recrystallized from acetonitrile): 317°-320° C. (with decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371710
Source datasetuspto-grants-1983_02
ORD IDord-70c6901ea92a41409ee491b1c2200142
Source noteuspto-grants-1983_02