Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | 2-Methylquinoline | HCID 7060 | — |
| Edukt | Ammonium Sulfate | HCID 6097028 | — |
| Katalysator | Ferrous sulfate heptahydrate | HCID 62662 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | (2-Methylquinolin-4-yl)methanol | HCID 10149033 | 27% |
Reaktionsschritte
To a solution of quinaldine (75 g, 0.523 mol) in methanol (1100 mL) and water (550 mL) at room temperature was added sulfuric acid (28 mL, 0.523 mol) followed by iron(II) sulfate heptahydrate. Nitrogen was bubbled into the solution for 20 min and ammonium sulfate (177 g, 1.56 mol) was added. The resultant mixture was stirred in a water bath (20° C.) under nitrogen for 4 hours and quenched with 10% sodium hydroxide (pH=9-10). Methanol was removed by concentration in vacuo and the resulting aqueous solution was extracted with ethyl acetate three times. The combined organic phase was filtered through silica gel and washed with water and brine, dried (MgSO4) and concentrated. Crystallization from ethyl acetate gave 2-methyl-4-hydroxymethylquinoline (24.6 g, 27%) as a solid. MS(NH3—CI): (M+H)+=174.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06858626B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-e61367d030e444008a55ea1f3a232f36 |
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| Quellennotiz | uspto-grants-2005_02 |
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