HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Sodium Methoxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 21387569 | HCID 21387569 | — |
| Product | Sodium Methoxide | HCID 10942334 | — |
| Product | HCID 15684250 | HCID 15684250 | — |
Reaction Steps
A solution of sodium methoxide was prepared by the addition of sodium hydride (0.72 g.) to methanol (25 ml.). (±) 3-α-Chlorobenzylpyridazine (prepared as described in Example 2) (4.1 g.) was heated at reflux in this solution for 2 hours and the mixture was evaporated to dryness. The residue was dissolved in a mixture of diethyl ether and water and the ethereal layer was separated, dried over sodium sulphate and evaporated to give a brown oil. Distillation of this oil gave (±) 3-α-methoxybenzylpyridazine (1.8 g.), b.p. 140°-180° C./0.2-0.4 mm.Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04067723 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-f4cea04706ea45b78a789c209f2a33a4 |
| Source note | uspto-grants-1978_01 |