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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Bromoquinoxaline | HCID 610939 | — |
| Reactant | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| Reactant | Tri-tert-butylphosphine tetrafluoroborate | HCID 2734635 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(Quinoxalin-6-yl)ethanone | HCID 22631249 | 51.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07205316B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-bf69d84871384c1eb6111f8fa0db674c |
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| Source note | uspto-grants-2007_04 |
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