Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Malonic Acid | HCID 867 | — |
| Reactant | N,N'-Dimethylurea | HCID 7293 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Dimethylbarbituric acid | HCID 69860 | 73.4% |
Reaction Steps
276 g (3.14 mol) of 1,3-dimethylurea and 376 g (3.62 mol) of malonic acid were dissolved in 600 ml of glacial acetic acid at 60° to 70° C. To the solution was added 1250 ml of acetic anhydride and the temperature was gradually raised to 90° C. After stirring for 6 hours, the reaction mixture was allowed to stand at room temperature overnight and then the glacial acetic acid and acetic anhydride were distilled off under reduced pressure. The residue was poured into 500 ml of ethanol while it was still hot, the crystals thus-deposited were collected by filtration and refluxed by heating in a mixture of 380 ml of concentrated hydrochloric acid and 400 ml of water for 2 hours. The mixture was allowed to stand under cooling with ice for 6 hours, the crystals thus-deposited were collected by filtration and washed with a small amount of ethanol to obtain 360 g of 1,3-dimethylbarbituric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05066573 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-aac6e0bdb5f144ddb0e83612a128d9d5 |
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| Source note | uspto-grants-1991_11 |
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