HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenylprop-2-Enal → 5-(3-Phenylprop-2-en-1-ylidene)-1,3-diazinane-2,4,6-trione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenylprop-2-Enal | HCID 307 | — |
| Reactant | Barbituric Acid | HCID 6211 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(3-Phenylprop-2-en-1-ylidene)-1,3-diazinane-2,4,6-trione | HCID 31907 | 96% |
Reaction Steps
Barbituric acid (10.0 g) was dissolved in water (150 ml) at reflux, and the solution was stirred vigorously and maintained at just below refluxing point while freshly distilled cinnamaldehyde (10.3 g) was added slowly: a yellow precipitate formed almost immediately. After the addition, the mixture was stirred and maintained at just below refluxing point for 1 hour to complete the reaction. The product was filtered off, washed several times with hot water and then with cold ethanol, and then dried to give yellow 5-cinnamylidenebarbituric acid (18 g, 96% theoretical yield) m.p. 268°-70° (decomp).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04124760 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-bf6416d54efc46fa958ac508dacac7a3 |
| Source note | uspto-grants-1978_11 |