HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dihydroxybenzaldehyde → HCID 136331475, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Reactant | Acetamide, N-(aminocarbonyl)-2-cyano- | HCID 74055 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136331475 | HCID 136331475 | 60.7% |
Reaction Steps
To 0.69 g (5 mmol) 3,4-dihydroxybenzaldehyde and 0.6 g (5.3 mmol) cyanoacetylurea in 40 ml ethanol was added 2 drops piperidine. The reaction mixture was refluxed for 2 hours, cooled, filtered and washed with cold ethanol to yield 0.75 g (60% yield) of a yellow-orange solid, m.p. 235° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05217999 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-58f0a97e644f4b60af08e49eec08a88e |
| Source note | uspto-grants-1993_06 |