Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Barbituric Acid | HCID 6211 | — |
| Reactant | HCID 23042627 | HCID 23042627 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 178513185 | HCID 178513185 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178514329 | HCID 178514329 | 90.2% |
Reaction Steps
29.9 g (0.22 mol) of aminoguanidine bicarbonate are dissolved in a mixture of 150 ml of water and 54 ml of 10N hydrochloric acid, and the solution is cooled to 0° C. by adding ice. 50 ml of an aqueous solution of sodium nitrite containing 30 g of dissolved sodium nitrite per 100 ml are added dropwise to this mixture in the course of about 15 minutes. After 5 minutes, a nitrite excess which may be present is removed using amidosulphonic acid. 25.6 g (0.2 mol) of barbituric acid are thrown into the solution of azidoformamidinium hydrochloride thus obtained, and the mixture is heated at 70° C. for 4 hours and at 95° for 1 hour. The solution is then cooled down to 0°-5°, the precipitate is filtered off with suction and washed with ice-cold water. Drying at 70° in a through-circulation cabinet gives 27.8 g (90.2%) of diazobarbituric acid of the formula ##STR8##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04942225 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-e71dab3ef48f4d188284691536cc039c |
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| Source note | uspto-grants-1990_07 |
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