Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2,4-Diamino-6-chloropyrimidine | HCID 67432 | — |
| Edukt | m-Chloroperbenzoic acid | HCID 70297 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | HCID 178507684 | HCID 178507684 | — |
Reaktionsschritte
75 g. of 2,4-diamino-6-chloropyrimidine are dissolved in 1500 ml. of ethanol at 35° C. The solution is cooled to -10° C. and a solution of 100 g. of 3-chloro-perbenzoic acid in 500 ml. of ethanol is slowly added dropwise in the course of 1 hour. The suspension is subsequently stirred at -10° C. for 7 hours and left to stand at 5° C. overnight. The suspension is neutralized with 24 g. of sodium hydroxide in 100 ml. of water. The solid material is filtered off and recrystallized from ethanol, there being obtained pure 2,4-diamino-6-chloropyrimidine-3-oxide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04220772 |
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| Quelldatensatz | uspto-grants-1980_09 |
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| ORD ID | ord-0cbe754051c04555a9debb952b65163a |
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| Quellennotiz | uspto-grants-1980_09 |
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