Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109866Generated: October 25, 2026

Acetic Anhydride → 4-Acetyl-3,4-dihydroquinoxalin-2(1H)-one

https://huagongshe.com/reaction/2109866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantDiisopropylethylamineHCID 81531—
Reactant2(1H)-Quinoxalinone, 3,4-dihydro-HCID 185949—
SolventDichloromethaneHCID 6344—
Product4-Acetyl-3,4-dihydroquinoxalin-2(1H)-oneHCID 2770825—

Reaction Steps

To a cold (0° C.) solution of 3,4-dihydroquinoxalin-2(1H)-one (1.0 g, 6.7 mmol; J. Med. Chem. 758, 1994) and N,N-diisopropyl-N-ethylamine (1.7 mL, 10.1 mmol) in dichloromethane (30 mL) under an atmosphere of nitrogen, acetic anhydride (0.76 mL, 8.1 mmol) was added and stirred at room temperature overnight. The resultant solution was concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with a 1% methanol in chloroform. Collection and concentration of appropriate fractions provided the acetylation product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517532B2
Source datasetuspto-grants-2009_04
ORD IDord-a03f1253aa264c2c937df899681758bf
Source noteuspto-grants-2009_04