HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774089Generated: October 25, 2026
Acetic Acid → 1-Benzyl-5-benzylidene-3-phenylbarbituric acid
https://huagongshe.com/reaction/1774089
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1-Benzyl-3-phenylbarbituric acid | HCID 21708751 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-Benzyl-5-benzylidene-3-phenylbarbituric acid | HCID 86730866 | 75% |
Reaction Steps
In a 300-ml glass flask equipped with a thermometer, a reflux condenser and a stirrer, 4.0 g of 1-benzyl-3-phenylbarbituric acid, 1.6 g of benzaldehyde, and 40 ml of acetic acid were put, the content was added with a drop of sulfuric acid, kept under stirring, the flask was heated so as to adjust the inner temperature to 100° C., and the content was continued to be stirred at 100° C. for 3 hours. The content was then cooled to 50° C., added with a mixed solution of 39 ml of isopropanol and 17 ml of water, stirred at 10° C. or below for one hour, filtered under suction to collect a deposited crystal, and the crystal was washed with methanol, to thereby obtain 3.9 g of 1-benzyl-5-benzylidene-3-phenylbarbituric acid as an intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09256099B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-29891404cbbb493095dee0f31f8f76ec |
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| Source note | uspto-grants-2016_02 |
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