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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373768Generated: October 30, 2026

Ethyl iodoacetate → HCID 19958587, compound

https://huagongshe.com/reaction/373768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl iodoacetateHCID 12183—
Reactant6,7-Dichloroquinoxalin-2(1H)-oneHCID 14423636—
SolventEthanolHCID 702—
ProductHCID 19958587HCID 1995858785%

Reaction Steps

Under a nitrogen atmosphere Na (0.25 g, 11 mmol) was dissolved in 100 ml of abs. ethanol and 6,7-dichloroquinoxalin-2(1H)-one (2.15 g, 10 mmol) (Liebigs Ann. Chem., (1982), 754) was added. The mixture was refluxed for 30 min., cooled to room temperature, and ethyl iodoacetate (1.43 ml, 12 mmol) was added. The clear reaction mixture was refluxed for 2 h during which time a precipitate was formed. This was filtered off, washed with abs. ethanol and dried to afford 2.56 g (85%) of 6,7-dichloro-1-ethoxycarbonylmethylquinoxalin-2(1H)-one. 1H-NMR (DMSO-d6):δ1.23 (t, 3H), 4.20 (q, 2H), 5.08 (s, 2H), 8.05 (s, 1H), 8.17 (s, 1H), 8.38 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166155
Source datasetuspto-grants-1992_11
ORD IDord-f8d086ae913e4bd7b81399eccba134ce
Source noteuspto-grants-1992_11