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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614165Generated: November 2, 2026

2(1H)-Quinoxalinone → 2-Chloroquinoxaline

https://huagongshe.com/reaction/1614165

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2(1H)-QuinoxalinoneHCID 14526—
ReactantPhosphorus oxychlorideHCID 24813—
SolventWaterHCID 962—
Product2-ChloroquinoxalineHCID 238938—

Reaction Steps

Quinoxalin-2-one (14.62 g, 100 mmol) was added to POCl3 (100 g, 0.65 mmol) and the mixture heated at reflux for 1.5 hours under N2. Upon cooling, the mixture was poured slowly, portionwise onto 700 ml of H2O. The black solution was extracted with CH2Cl2 (2×250 ml). The combined CH2Cl2 portions were washed with H2O, dried over Na2SO4, filtered, and evaporated to give a brown, solid 2-chloroquinoxaline. A portion of said product (4.00 g, 24.3 mmol) was combined with 5 ml of 1N HCl, and NaN3 (1.89 g, 29.1 mmol) in 220 ml of abs EtOH and heated at reflux for 7 hours. The mixture was allowed to cool overnight, which led to precipitation of yellow-brown needles of tetrazolo[1,5-a]quinoxaline (19).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05196421
Source datasetuspto-grants-1993_03
ORD IDord-66781d67892d46d7ab46d183a4891913
Source noteuspto-grants-1993_03