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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389252Generated: October 31, 2026

Phenacyl bromide → Quinoxaline

https://huagongshe.com/reaction/2389252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantO-PhenylenediamineHCID 7243—
ReactantDiisopropylethylamineHCID 81531—
SolventEthanolHCID 702—
ProductQuinoxalineHCID 7045—

Reaction Steps

To a magnetically stirred solution of the appropriate α-bromoacetophenone (1 eq) in 5 ml of ethanol was added the appropriate 1,2-phenylenediamine (2.7 eq), followed by DIPEA (3.4 eq). The resultant solution was stirred at room temperature overnight with an air atmosphere. The reaction was concentrated, then purified by reverse phase chromatography on a C-18 column using a 0 to 90% gradient of CH3CN in water, with both containing 0.05% TFA. Product containing fractions were lyophilized to give a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273743B2
Source datasetuspto-grants-2012_09
ORD IDord-21942672486345f8ac1ca8ebd13f72d5
Source noteuspto-grants-2012_09