Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968745Generated: October 26, 2026

Selenious Acid → (6-Chloro-3-formyl-quinoxalin-5-yl)-acetic acid methyl ester

https://huagongshe.com/reaction/1968745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSelenious AcidHCID 1091—
Reactant(6-Chloro-3-methyl-quinoxalin-5-yl)-acetic acid methyl esterHCID 66882129—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product(6-Chloro-3-formyl-quinoxalin-5-yl)-acetic acid methyl esterHCID 8625393881%

Reaction Conditions

Temperature100 °C

Reaction Steps

Selenious acid (645 mg, 5.00 mmol, 1.1 equiv) was added to a solution of (6-chloro-3-methyl-quinoxalin-5-yl)-acetic acid methyl ester in dioxane (30 ml). The reaction mixture was heated to 100° C. After 60 minutes, an additional portion of selenious acid (645 mg) was added, and heating was continued for another 60 minutes. After cooling, the reaction mixture was diluted with water, filtered, and extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified via flash chromatography (gradient of hexane/EtOAc 100:0 to 80:20) to afford the title compound (966 mg, 81%). MS (ES+): 264 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426440B2
Source datasetuspto-grants-2013_04
ORD IDord-f86a5861158e4eca900ae4f03c1b29a4
Source noteuspto-grants-2013_04