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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789997Generated: October 29, 2026

Butanedione → HCID 22037030, compound

https://huagongshe.com/reaction/1789997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanedioneHCID 650—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium PyrosulfiteHCID 656671—
ReactantEthyl 2,3-diaminobenzoateHCID 11171330—
SolventWaterHCID 962—
ProductHCID 22037030HCID 2203703067.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

2,3-Butanedione (0.0776 mol) was added at room temperature to a solution of sodium pyrosulfite (0.1 mol) in water (75 ml). The mixture was heated to 70° C. and then added to a solution of ethyl 2,3-diaminobenzoate (0.0776 mol) in water (75 ml). The mixture was stirred at 100° C. for 12 hours, cooled, basified with K2CO3 10% and =extracted with EtOAc. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated. The residue (17.5 g) was purified by column chromatography over silica gel (eluent: CH2Cl2/EtOAc 93/7; 20–45 μm). The pure fractions were collected and the solvent was evaporated, yielding 12 g (67%) of ethyl 2,3-dimethyl-5-quinoxalinecarboxylate (interm. 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071192B1
Source datasetuspto-grants-2006_07
ORD IDord-a0f99a5dfa9a45848a8856bf58a18c6e
Source noteuspto-grants-2006_07