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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044945Generated: October 25, 2026

Ethyl Acetate → 2-(Bromomethyl)-3-(2-chlorophenyl)-5-nitroquinoxaline

https://huagongshe.com/reaction/2044945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3-Nitro-1,2-phenylenediamineHCID 4359525—
Reactant3-Bromo-1-(2-chlorophenyl)propane-1,2-dioneHCID 57556170—
Product2-(Bromomethyl)-3-(2-chlorophenyl)-5-nitroquinoxalineHCID 57707807—

Reaction Steps

To a solution of 3-bromo-1-(2-chlorophenyl)propane-1,2-dione (Prepared in Example 81, 4.2971 g, 16.4325 mmol) in ethyl acetate (109.55 mL, 16.433 mmol) was added 3-nitro-1,2-phenylenediamine (2.5165 g, 16.433 mmol) at room temperature and the resulting red mixture was stirred at room temperature. After 26 h of stirring at room temperature, the mixture was concentrated under reduced pressure to give 2-(bromomethyl)-3-(2-chlorophenyl)-5-nitroquinoxaline including its regioisomer as a red syrup: LC-MS (ESI) m/z 378.0 and 379.9 [M+H]+. The crude product as a red syrup was carried on crude without purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586739B2
Source datasetuspto-grants-2013_11
ORD IDord-38ae53c62c2b40e48d0a3a5590d77bc1
Source noteuspto-grants-2013_11