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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709221Generated: October 31, 2026

Hydrochloric Acid → HCID 19827795, compound

https://huagongshe.com/reaction/1709221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 19827831HCID 19827831—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
ProductHCID 19827795HCID 1982779523%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 1.6 g (5,0 mmol) N-diphenylmethyl-2-amino-4fluoroaniline in 100 ml ethyl acetate was hydrogenated at atm. pressure by using 5% Pd/C (100 mg) as a catalyst. The reaction mixture was filtered and 4.2 ml (30 mmol) dry triethylamine was added. 3.4 ml (30 mmol) ethyl oxalylchloride was added dropwise, and the reaction mixture was stirred for 1 h. The reaction mixture was filtered and evaporated in vacuo to give an oil. A mixture of the oil, 40 ml 1N hydrochloric acid and 60 ml ethanol was stirred at 80° C. for 4 h. After cooling to 25° C. 50 ml H2O was added, and the precipitate was filtered off. The crude product was dissolved in 20 ml ethanol, filtered and evaporated in vacuo to give an oil. The oil was stirred with 30 ml water for 1 h. The product was filtered off and dried to give 0.4 g (23%) 1-diphenylmethyl-6-fluoroquinoxaline-2,3(1H,4H)-dione. M.p. 143.8° C., 1H-NMR (CDCl3): 8.5-6.5 (3H, m), 7.2 (10H, s) 3.8 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04948794
Source datasetuspto-grants-1990_08
ORD IDord-830e4b639f0547fba20040522dc6bee1
Source noteuspto-grants-1990_08