HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicylic Acid → HCID 22613512, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicylic Acid | HCID 338 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzoylhydrazine | HCID 11955 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 22613512 | HCID 22613512 | 67% |
Reaction Steps
13.6 g (0.1 mol) of benzhydrazide and 13.8 g (0.1 mol) of salicylic acid are initially introduced into 200 ml of chlorobenzene and the mixture is heated to the boil. After adding 3.0 g (0.038 mol) of pyridine, 13.1 g (0.11 mol) of thionyl chloride are added dropwise over the course of 1 hour. The reaction starts immediately whilst the product separates out as a white precipitate. After cooling, the mixture is filtered and the product is washed with methanol and dried. N-Salicyloyl-N'-phenyl-hydrazine of melting point 259° C is thus obtained in 67% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002680 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-728115499bfc4490906a9de7792bcc91 |
| Source note | uspto-grants-1977_01 |