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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271385Generated: November 1, 2026

6-Bromoquinoxaline → 1-(Quinoxalin-6-yl)ethanone

https://huagongshe.com/reaction/1271385

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-BromoquinoxalineHCID 610939—
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product1-(Quinoxalin-6-yl)ethanoneHCID 2263124951.1%

Reaction Steps

A solution of 6-bromo-quinoxaline (261 mg, 1.25 mmol), 1-ethoxyvinyltri-n-butyltin (0.47 mL, 1.4 mmol), palladium(II) acetate (16 mg) and tri-t-butylphosphonium tetrafluoroborate (41 mg) in anhydrous DMF (4 mL) under a nitrogen atmosphere was heated at 120° C. for 1 hr. The reaction mixture was cooled to ambient temperature and partitioned between ethyl acetate (25 mL) and H2O (10 mL). The organic extraction was washed with brine, dried (MgSO4), filtered, and concentrated. The concentrate was chromatographed on silica gel eluting with ethyl acetate:hexanes (1:1) to provide 110 mg of the title compound. 1H NMR (300 MHz, CDCl3) δ 2.79 (s, 3 H), 8.18 (d, J=9 Hz, 1 H), 8.36 (dd, J=9 Hz, J=3 Hz, 1 H), 8.70 (d, J=3 Hz, 1 H), 8.95 (s, 2 H); MS (DCl/NH3) m/z 173 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205316B2
Source datasetuspto-grants-2007_04
ORD IDord-bf69d84871384c1eb6111f8fa0db674c
Source noteuspto-grants-2007_04