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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-Bromo-2-chloroquinoxaline | HCID 4913253 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Chloroform isopropyl alcohol | HCID 21906603 | — |
| Product | 2-((7-Bromoquinoxalin-2-yl)oxy)ethanol | HCID 59710030 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07368445B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-a4889f522b0b4858975f0b7fa5b221b5 |
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| Source note | uspto-grants-2008_05 |
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