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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44187Generated: October 27, 2026

Sodium Iodide → 6-Bromo-1,2,3,4-tetrahydroquinoxalin-2-one

https://huagongshe.com/reaction/44187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
ReactantN-(2-Amino-4-bromophenyl)-2-chloroacetamideHCID 66911433—
SolventAcetonitrileHCID 6342—
Product6-Bromo-1,2,3,4-tetrahydroquinoxalin-2-oneHCID 6691130734.1%

Reaction Steps

A mixture of N-(2-amino-4-bromophenyl)-2-chloroacetamide (4.5 g, 17.0 mmol), sodium iodide (101 mg, 2.0 mmol) and sodium carbonate (3.6 g, 33.8 mmol) in 300 ml acetonitrile was refluxed overnight under an atmosphere of nitrogen. Then the acetonitrile was removed under vacuum. The resulting solid was suspended in 150 ml water acidified to pH 5-6 with 1 N HCl. Extraction with ethyl acetate, washing of the combined organic layers with brine, drying over MgSO4, removing the solvent under reduced pressure and purification of the crude product by flash chromatography on silica gel (petroleum ether/ethyl acetate, 1.5/1) yielded 6-bromo-3,4-dihydroquinoxalin-2(1H)-one (1.3 g, 5.8 mmol, 34%) as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541404B2
Source datasetuspto-grants-2013_09
ORD IDord-42eee9138f1c4f8c95f371ff90bc6edb
Source noteuspto-grants-2013_09