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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzaldehydeHCID 240—
ReactantSulfuric AcidHCID 1118—
Reactant1-Benzyl-3-phenylbarbituric acidHCID 21708751—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product1-Benzyl-5-benzylidene-3-phenylbarbituric acidHCID 8673086675%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09256099B2
Source datasetuspto-grants-2016_02
ORD IDord-29891404cbbb493095dee0f31f8f76ec
Source noteuspto-grants-2016_02