Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Solketal | HCID 7528 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 3-Methoxy-2-nitropyridine | HCID 556063 | — |
| Lösungsmittel | Hexamethylphosphoramide | HCID 12679 | — |
| Produkt | 3-[(3-Methoxypyridin-2-yl)oxy]propane-1,2-diol | HCID 13195074 | — |
Reaktionsschritte
26.5 g of sodium hydride are added in the course of one hour to a mixture of 161 g of 3-methoxy-2-nitropyridine and 144 g of 2,2-dimethyl-5-hydroxymethyl-1,3-dioxolane in 1,000 ml of hexamethylphosphoric acid triamide, with stirring; by means of cooling, the temperature is kept at 0°-10° during the addition. The reaction mixture is then stirred for a further 5 hours with ice-cooling and then for 15 hours at room temperature. The reaction mixture is poured onto ice and extracted with diethyl ether. The organic extract is washed with a concentrated aqueous solution of sodium chloride, dried and evaporated. The residue is dissolved in 1,000 ml of ethanol, 100 ml of 2 N hydrochloric acid are added and the mixture is left to stand for 8 hours. After evaporating off the solvent, the residue is rendered alkaline with a concentrated solution of sodium hydroxide in water and extracted with ethyl acetate. Evaporating off the solvent yields a crude product from which crystalline 3-(3-methoxy-2-pyridyloxy)-1,2-propanediol with a melting point of 62°-65° is obtained on the addition of diethyl ether.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04264599 |
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| Quelldatensatz | uspto-grants-1981_04 |
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| ORD ID | ord-cb9ffa13d32d4036b5c5f24a2f2a61e9 |
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| Quellennotiz | uspto-grants-1981_04 |
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