Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515347Generated: October 27, 2026

Ethanol → 1-(3,4-Dihydroquinoxalin-1(2h)-yl)ethanone

https://huagongshe.com/reaction/1515347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1,2,3,4-TetrahydroquinoxalineHCID 77028—
SolventAcetic AnhydrideHCID 7918—
SolventSodium HydroxideHCID 14798—
Product1-(3,4-Dihydroquinoxalin-1(2h)-yl)ethanoneHCID 241507—

Reaction Steps

To a solution of 1,2,3,4-tetrahydroquinoxaline obtained in Reference Example 26 (360 mg) in ethanol (10 ml), acetic anhydride (254 μl) was added dropwise under ice cooling and stirred at room temperature for 10 minutes. The reaction mixture was diluted with 1M aqueous sodium hydroxide (10 ml) and extracted with chloroform. The organic layer was washed with brine and dried over anhydrous sodium sulfate. The desiccant was filtered off and the solvent was distilled off under reduced pressure to give the titled compound, i.e., 1-acetyl-1,2,3,4-tetrahydroquinoxaline (494 mg) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222417B2
Source datasetuspto-grants-2012_07
ORD IDord-a3fe6206b0324603b0201b52ce20cac5
Source noteuspto-grants-2012_07