Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581781Generated: October 27, 2026

Methylglyoxal → HCID 135407226, compound

https://huagongshe.com/reaction/581781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylglyoxalHCID 880—
ReactantSodium BicarbonateHCID 516892—
Reactant2,3-DiaminophenolHCID 579937—
SolventAcetic AcidHCID 176—
SolventSodium AcetateHCID 517045—
ProductHCID 135407226HCID 135407226—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of 2,3-diaminophenol (2.93 g) in 2M aqueous acetic acid solution (47 ml) and 4M aqueous sodium acetate solution (29 ml) was added 40% aqueous pyruvic aldehyde solution (3.79 ml) at 60° C. The reaction mixture was stirred at 60° C. for 40 minutes. After cooling the reaction mixture was adjusted to pH 8 with saturated sodium hydrogen carbonate and extracted with dichloromethane (50 ml) twice. The organic layer was washed with saturated sodium hydrogen carbonate, water and brine. After dried over anhydrous magnesium sulfate, the solution was evaporated in vacuo. The residue was purified by flash column chromatography (silica gel 450 ml) eluting with n-hexane/ethyl acetate (5/1, V/V) to give 8-hydroxy-2-methylquinoxaline (the less polar product) as crystals and with n-hexane/ethyl acetate (3/1, V/V) to give 8-hydroxy-3-methylquinoxaline (the more polar product) as crystals. The former was washed with n-hexane to afford pale yellow crystals (1.27 g). The latter was washed with isopropyl ether to afford pale yellow crystals (1.30 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922711
Source datasetuspto-grants-1999_07
ORD IDord-95e46af0b1ba439d913275966483cd95
Source noteuspto-grants-1999_07