HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 6,7-Dichloro-2,3-dimethoxy-5-methylquinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 5-Methyl-2,3,6,7-tetrachloroquinoxaline | HCID 10678123 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6,7-Dichloro-2,3-dimethoxy-5-methylquinoxaline | HCID 10802193 | 100% |
Reaction Steps
A solution of sodium methoxide (38 ml, 25% solution in methanol, 175 mmol) was added over 10 minutes to a solution of 5-methyl-2,3,6,7-tetrachloroquinoxaline (from step (e), 21 g, 74 mmol) in dry tetrahydrofuran (200 ml) at 20° C. There was a mildly exothermic reaction followed by formation of a precipitate. After 1 h the mixture was diluted with ethyl acetate (3 L), washed with water (1 L), dried (MgSO4) and concentrated under reduced pressure to give 6,7-dichloro-2,3-dimethoxy-5-methylquinoxaline (20.3 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05852016 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-eaa4b76818d4427f99a4a85a89f2bb7b |
| Source note | uspto-grants-1998_12 |