HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505235Generated: October 31, 2026
Vinylidene chloride → 7-Chloro-2-methyl-8-(2,2,2-trichloroethyl)quinoxaline
https://huagongshe.com/reaction/505235
Participants
| Role | Name | HCID | Charge |
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| Reactant | Vinylidene chloride | HCID 6366 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 6-Chloro-3-methylquinoxalin-5-amine | HCID 66883318 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-Chloro-2-methyl-8-(2,2,2-trichloroethyl)quinoxaline | HCID 66882040 | 56% |
Reaction Steps
Tert-butylnitrite (2.74 g, 26.60 mmol, 1.5 equiv) was added to a suspension of copper(II) chloride (2.86 g, 21.28 mmol, 1.2 equiv) in anhydrous acetonitrile (25 ml). 1,1-Dichloroethene (25.8 g, 266 mmol, 15 equiv) and a solution of 6-chloro-3-methyl-quinoxalin-5-ylamine (3.43 g, 17.74 mmol) in anhydrous acetonitrile (16 ml) were added. After 4 hours at room temperature, concentrated aqueous NH4Cl solution and EtOAc were added. The mixture was filtered and extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified via flash chromatography (gradient of hexane/EtOAc 100:0 to 90:10) to afford the title compound (3.08 g, 56%) as an oil. 1H NMR (400 MHz, CDCl3): δ=8.71 (s, 1H), 8.02 (d, J=8.8 Hz, 1H), 7.74 (d, J=8.8 Hz, 1H), 4.98 (s, 2H), 2.77 (s, 3H). MS (ES+): 310 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781438B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-a159d9c857e24c428de49b07c9cda041 |
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| Source note | uspto-grants-2010_08 |
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