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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703628Generated: October 31, 2026

3-Phenylprop-2-Enal → 5-(3-Phenylprop-2-en-1-ylidene)-1,3-diazinane-2,4,6-trione

https://huagongshe.com/reaction/1703628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Phenylprop-2-EnalHCID 307—
ReactantBarbituric AcidHCID 6211—
SolventWaterHCID 962—
Product5-(3-Phenylprop-2-en-1-ylidene)-1,3-diazinane-2,4,6-trioneHCID 3190796%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04124760
Source datasetuspto-grants-1978_11
ORD IDord-bf6416d54efc46fa958ac508dacac7a3
Source noteuspto-grants-1978_11