Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175690Generated: October 29, 2026

O-Phenylenediamine → 2(1H)-Quinoxalinone, 3,4-dihydro-

https://huagongshe.com/reaction/2175690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
ReactantEthyl bromoacetateHCID 7748—
ReactantTriethylamineHCID 8471—
SolventDimethylformamideHCID 6228—
Product2(1H)-Quinoxalinone, 3,4-dihydro-HCID 18594938%

Reaction Steps

To a solution of o-phenylenediamine (1.08 g, 10 mmol) in DMF (50 mL) was added Et3N (2.9 mL, 21 mmol), and ethyl 2-bromoacetate (1.2 mL, 11 mmol). The reaction mixture was stirred at room temperature for 16 h, then at 80° C. for 3 h. The DMF was evaporated under reduced pressure and the reaction mixture partitioned between H2O and EtOAc. The EtOAc layer was washed with sat. NaHCO3, brine, and dried over Na2SO4. The solvent was evaporated under reduced pressure and the crude residue purified by flash chromatography eluting with petroleum ether/EtOAc (4/1) to give 3,4-dihydroquinoxalin-2(1H)-one (560 mg, 38%) as yellow solid. LC-MS (ES-API); rt 7.40 min; m/z calculated for C8H8N2O [M+H]+ 149.0, found 149.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062076B2
Source datasetuspto-grants-2015_06
ORD IDord-41db82ad277b476eaf9f89c964a0c614
Source noteuspto-grants-2015_06