HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 3-Chloro-6-methoxypyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | 3-Chloro-6-methoxypyridazine | HCID 74403 | — |
Reaction Steps
Sodium (4.8 g, 0.21 mol) is added portion-wise to MeOH (200 ml) with stirring. After a clear solution is formed, it is added slowly to a solution of 3,6-dichloro-pyridazine (29.6 g, 0.2 mol) in MeOH (200 ml). After addition, the mixture is heated at reflux for 3 h, then cooled and concentrated under reduced pressure. EtOAc and water are added. The organic layer is separated, dried and concentrated under reduced pressure to give 26.4 g of 3-chloro-6-methoxy-pyridazine as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338591B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-b31924a88e5548a1a432133a8f309854 |
| Source note | uspto-grants-2012_12 |