HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dihydroxybenzaldehyde → 3,4-Dihydroxybenzylidenecyanoacethydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Reactant | Cyanoacetic acid hydrazide | HCID 8820 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3,4-Dihydroxybenzylidenecyanoacethydrazide | HCID 53722048 | 50.2% |
Reaction Steps
To 0.69 g (5 mmol) 3,4-dihydroxybenzaldehyde and 0.55 g (5.5 mmol) cyanoacethydrazide in 40 ml ethanol was added 2 drops piperidine. After 2½ hours of reflux, the reaction mixture was cooled, filtered and washed with cold ethanol to give 0.55 g (50% yield) of product, an orange solid, m.p. 220° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE038761E1 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-dd7ce8c852b5480da9966d553f38d757 |
| Source note | uspto-grants-2005_07 |