HuagongsheHuagongshe Chemistry Print Report · For research reference only
Magnesium monoxide → 3-Benzylpyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Magnesium monoxide | HCID 6850729 | — |
| Reactant | HCID 15684248 | HCID 15684248 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Benzylpyridazine | HCID 598149 | 93.8% |
Reaction Steps
A solution of (±) 3-α-chlorobenzylpyridazine (2.05 g.) in ethanol (50 ml.) was treated with hydrogen, in the presence of magnesium oxide (0.4 g.) and palladium on charcoal (5% Pd; 0.2 g.), for 1 hour at ambient temperature and normal atmospheric pressure. The solution was then filtered and the filtrate was evaporated to dryness. The residue was dissolved in hot chloroform (100 ml.), cooled, washed with water (50 ml.), dried over magnesium sulphate and evaporated to give 3-benzylpyridazine (1.6 g.), m.p. 61°-64° C., in the form of a light brown coloured solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04067723 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-ab703a07c09346e8ab24ce79bed21700 |
| Source note | uspto-grants-1978_01 |