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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699734Generated: October 31, 2026

Toluene → HCID 18369162, compound

https://huagongshe.com/reaction/1699734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantIodoethaneHCID 6340—
ReactantPotassium NitrateHCID 24434—
ReactantHCID 387928HCID 387928—
CatalystSilver(II) oxideHCID 92152—
SolventSulfuric AcidHCID 1118—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 18369162HCID 1836916241%

Reaction Steps

To a solution of ethyl 3,4-dihydro-3-oxo-6-trifluoromethylquinoxaline-2-carboxylate (500 mg, 1.75 mmol) in concentrated sulfuric acid (5 ml) was added potassium nitrate (354 mg, 3.50 mmol) at 40° C., and the mixture was stirred for 3 hours at the same temperature. The reaction mixture was poured into ice water (100 ml), which was extracted with ethyl acetate. After dried over anhydrous sodium sulfate, solvent was distilled off. Silver oxide (I)(811 mg, 3.50 mmol) was added to the residue obtained which was suspended into toluene (10 ml). Then, iodoethane (280 μl, 3.50 mmol) was added dropwise at 100° C. and the mixture was refluxed for 2 hours. After cooling, the insolubles were filtered off using celite and the solvent was distilled off. The residue obtained was submitted to silica gel column chromatography [hexane-ethyl acetate=8:1] to obtain 255 mg of the title compound as yellowish brown oily product. Yield 41%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06348461B1
Source datasetuspto-grants-2002_02
ORD IDord-394f1e170aba4861b7e4218678eeb83c
Source noteuspto-grants-2002_02