HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 20144038, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Cyanobenzoyl chloride | HCID 80172 | — |
| Reactant | α-Pyridoin | HCID 95624 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 20144038 | HCID 20144038 | — |
Reaction Steps
To 2.14 g (0.01 mole) of α-pyridoin in 50 ml of acetonitrile was added 0.80 g (0.01 mole) of pyridine and then 1.65 g (0.01 mole) of p-cyanobenzoyl chloride portionwise with stirring. Stirring was continued for 1/2 hour. Then 150 ml of dichloromethane was added, the organic phase washed thoroughly with water, dried and evaporated to an oily solid residue. The residue was stirred with 80% hexane and 20% acetone to obtain a solid, 1.7 g (50%). After recrystallization from hexane-acetone, 0.9 g (53%), m.p., 152°-154° C., of NA-VI was recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04737439 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-56438169cbc84ff6ba4d7c1f315f0867 |
| Source note | uspto-grants-1988_04 |