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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957121Generated: October 31, 2026

Hydrochloric Acid → HCID 10691461, compound

https://huagongshe.com/reaction/1957121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
Reactant5-Amino-6,7-dichloro-2,3-dimethoxyquinoxalineHCID 10606620—
ReactantSodium NitriteHCID 23668193—
SolventAcetoneHCID 180—
ProductHCID 10691461HCID 1069146132%

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Amino-6,7-dichloro-2,3-dimethoxyquinoxaline (from (c) above) (38.12 g, 0.14 mol) was dissolved in acetone (2 L) and cooled to 0° C. Whilst being agitated using a mechanical stirrer, the solution was treated first with 2M hydrochloric acid (396 mL, 0.79 mol) and then dropwise with 1M aqueous sodium nitrite (208 mL, 0.208 mol), maintaining the temperature of the mixture at 0° C. After the additions were complete, the mixture was stirred for 15 minutes, then treated with 5M aqueous potassium iodide (278 mL, 1.39 mol) maintaining the temperature below 5° C. The mixture was then allowed to warm to 10° C. over 30 minutes. The acetone was removed under reduced pressure and the residue partitioned between water and ethyl acetate (total of 4 L). The organic solution was washed with 10% aqueous sodium bisulphite, saturated aqueous sodium bicarbonate, dried (MgSO4), and concentrated under reduced pressure. Purification by flash chromatography (eluting with toluene) gave 6,7-dichloro-2,3-dimethoxy-5-iodoquinoxaline (16.9 g, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783572
Source datasetuspto-grants-1998_07
ORD IDord-2bed7cece5294ae288f1b9ee2e9694c5
Source noteuspto-grants-1998_07