Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Phenazine | HCID 4757 | — |
| Edukt | Propylene Oxide | HCID 6378 | — |
| Edukt | Ethylene glycol diethyl ether | HCID 12375 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Produkt | 5,10-Bis(2-hydroxypropyl)-5,10-dihydrophenazine | HCID 18520843 | — |
Reaktionsschritte
40 g (0.22 mol) of phenazine are dissolved in 500 ml of anhydrous 1,2-diethoxyethane at 80° C. under an argon atmosphere. 14 g of sodium are added. The reaction mixture is stirred vigorously under reflux at 120° C. for 24 hours and cooled to room temperature. A solution of 39 g (0.66 mol) of 1,2-propylene oxide in 50 ml of 1,2-diethoxyethane is poured into the resultant 5,10-disodium 5,10-dihydrophenazine suspension. After the reaction mixture has been stirred at room temperature for 1 hour and at 50° C. for 2 hours, the precipitate is removed by filtration. All the anhydrous 1,2-diethoxyethane is distilled off on a rotary evaporator and used for the further synthesis. The solid residue, together with filtered-off precipitate, is mixed with 500 ml of methanol, and the mixture is stirred for 30 minutes. The solution is then evaporated on a rotary evaporator and transferred into a separating funnel, chloroform is added, and the mixture is washed a number of times with water and dried using magnesium sulphate. After the solvent has been distilled off, the product is purified by chromatography (silica gel column; cyclohexane/dioxane=1/1) and recrystallized from 150 ml of an acetone/water (2/1) mixture. The yield of the pale-green crystals is 22.5 g.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06569361B1 |
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| Quelldatensatz | uspto-grants-2003_05 |
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| ORD ID | ord-d148991165cd4152b462abd82e05cf84 |
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| Quellennotiz | uspto-grants-2003_05 |
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