HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetonitrile → HCID 63204030, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetonitrile | HCID 8794 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | 3-Chloro-6-methylpyridazine | HCID 227254 | — |
| Reactant | HCID 11127164 | HCID 11127164 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 63204030 | HCID 63204030 | — |
Reaction Steps
To a solution of 6.5 g (0.05 mole) of 3-chloro-6-methylpyridazine and 7.0 g (0.06 mole) of phenylacetonitrile in 50 ml of dry benzene was gradually added 4.0 g of pulverized sodium amide. The mixture was then slowly heated to 80° to 90° C. and maintained at this temperature for one hour. The reaction mixture was thereafter treated in the same manner as in the preparation of 2-phenyl-2-(3-pyridazinyl)-acetonitrile (see Example 1). The resulting product was recrystallized from a mixture of ethanol and isopropyl ether, giving 6.0 g (58% yield) of 2-phenyl-2-(6-methyl-3-pyridazinyl acetonitrile as pale yellow crystals, m.p. 121°-122° C. (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04242512 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-c23f1db0bca646eabdd331a52be916bb |
| Source note | uspto-grants-1980_12 |