Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Peracetic Acid | HCID 6585 | — |
| Edukt | 2,4-Diamino-6-chloropyrimidine | HCID 67432 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | HCID 178507684 | HCID 178507684 | — |
Reaktionsschritte
144.5 G. of 2,4-diamino-6-chloropyrimidine are suspended in 2000 ml. of ethanol. The suspension is warmed to 35° C. while stirring (about 15 minutes), the greater part of the material passing into solution. This mixture is then cooled down to 6°-8° C. and at this temperature there are added dropwise within 40 minutes 175 ml. of 40% peracetic acid in glacial acetic acid. After completion of the addition, the mixture is stirred at 6°-8° C. for a further 30 minutes. Thereafter, the mixture is left to warm up to room temperature, and stirred at this temperature for 3 hours. 2000 Ml. of petroleum ether are added, the mixture is stirred for 1 hour and then left to stand overnight. The separated precipitate is filtered off, back-washed with 200 ml. of petroleum ether and dried under reduced pressure, there being obtained 2,4-diamino-6-chloro-pyrimidine-3-oxide. Recrystallization yields analytically pure product having a melting point of 193° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04150131 |
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| Quelldatensatz | uspto-grants-1979_04 |
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| ORD ID | ord-8e32e366e0bb464a9c23ca4d3634022b |
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| Quellennotiz | uspto-grants-1979_04 |
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