Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propanedioyl dichloride | HCID 74269 | — |
| Reactant | N'-Butyl-N-phenylcarbamimidic acid | HCID 96940 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-Butyl barbituric acid | HCID 74771 | — |
Reaction Steps
A quantity of 3.85 g of 1-t.butyl-3-phenylurea is stirred at 0° C. in 50 ml of dry diethyl ether. 1.95 ml of malonylchloride are slowly added dropwise to this solution. After the addition of a little triethylamine the reaction mixture is slowly heated to approximately 30° C. After 2 hours 50 ml of water are added. The ether layer is separated, washed with water, dried and evaporated. After recrystallisation from ethanol, 1-phenyl-3-t.butyl-barbituric acid is obtained in a yield of 0.6 g; melting-point 118°-125° C. The resulting product is acetylated as described in Example III, the title compound (28) being obtained; melting-point 145°-148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05164396 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-53e4070c15a24777ab2ebffe8e32e760 |
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| Source note | uspto-grants-1992_11 |
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