Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 6,7-Dimethoxy-2,3-dimethylquinoxaline | HCID 3082342 | — |
| Product | HCID 21415702 | HCID 21415702 | — |
Reaction Steps
5.5 g (0.025 mol) of 2,3-dimethyl-6,7-dimethoxyquinoxaline are dissolved in 30 ml of methyl iodide, in a 100 ml stirred autoclave. This solution is warmed to 100° C over the course of 24 hours. whilst stirring, the pressure rising to about 7 atmospheres gauge. After cooling to room temperature, the yellow precipitate is filtered off, rinsed with a little dry acetone and dried. Yield about 6.5 g, corresponding to 72% of theory. Melting point 210° to 212° C (decomposition). The IR (KBr) and NMR (DMSO-d6) spectra are in agreement with the postulated structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04043819 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-c9a94e0fed454d9c888594dcd4af5fea |
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| Source note | uspto-grants-1977_08 |
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