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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221152Generated: October 26, 2026

Ethylene Glycol → 2-((7-Bromoquinoxalin-2-yl)oxy)ethanol

https://huagongshe.com/reaction/2221152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantSodium hydrideHCID 24758—
Reactant7-Bromo-2-chloroquinoxalineHCID 4913253—
SolventDimethylformamideHCID 6228—
SolventChloroform isopropyl alcoholHCID 21906603—
Product2-((7-Bromoquinoxalin-2-yl)oxy)ethanolHCID 5971003085%

Reaction Conditions

Temperature0 °C

Reaction Steps

Suspend sodium hydride (310 mg, 13 mmol) in a solution of ethylene glycol (800 mg, 13 mmol) in DMF (50 mL) previously cooled to 0° C. Allow the mixture to warm to room temperature and stir for 30 min. Add 7-bromo-2-chloroquinoxaline (610 mg, 2.5 mmol) and stir the resulting mixture for 2 h at room temperature. Dilute the mixture with 3:1 chloroform/isopropyl alcohol and wash the resulting solution with saturated sodium chloride solution. Dry and concentrate the organic phase in vacuo and purify the residue via silica gel chromatography to provide 564 mg (85%) of the titled compound. MS ES+ m/e 268 (M+1). 1H NMR (400 MHz, CDCl3) δ 8. (s, 1H), 8.0 (d, J=2.0 Hz, 1H), 7.90 (dd, J=8.8, 2.0 Hz, 1H), 7.7 (d, J=8.8 Hz, 1H), 4.6 (t, J=4.8 Hz, 2H), 4.39 (t, J=4.8 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368445B2
Source datasetuspto-grants-2008_05
ORD IDord-a4889f522b0b4858975f0b7fa5b221b5
Source noteuspto-grants-2008_05