Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrogen Peroxide | HCID 784 | — |
| Edukt | 2,3,5-Trimethylpyridine | HCID 12759 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 2,3,5-Trimethyl-1-oxidopyridin-1-ium | HCID 10486907 | — |
Reaktionsschritte
420 ml of 30% hydrogen peroxide are added dropwise at room temperature to 246.4 g of 2,3,5-collidine and 2400 ml of glacial acetic acid. The solution is stirred at 80° overnight. The reaction mixture is then cooled to 40° , a further 420 ml of 30% hydrogen peroxide are added thereto and the mixture is heated to 80° for a further 24 hours. After evaporation in vacuo the residue is dissolved in 300 ml of water, whereupon the solution is made basic with conc. sodium hydroxide solution while cooling, saturated with sodium chloride and extracted three times with 1 1 of methylene chloride. The organic phases are dried over sodium sulphate and evaporated in vacuo. The residue is crystallized from ether/petroleum ether; there is obtained 2,3,5-trimethylpyridine 1-oxide of melting point 42°-44°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04766133 |
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| Quelldatensatz | uspto-grants-1988_08 |
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| ORD ID | ord-edb4cdf3720449e2bd4e656c8d55258c |
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| Quellennotiz | uspto-grants-1988_08 |
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