Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Bromopentane | HCID 8057 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 1-(2-Furyl)ethanol | HCID 107243 | — |
| Katalysator | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Produkt | 2-(1-Pentoxyethyl)furan | HCID 20269896 | — |
Reaktionsschritte
Ten grams of the distilled 1-furylethanol (0.089 mole) is charged to a reactor with 0.61 g (2 mole percent) tetrabutylammonium bisulfate and 19.2 g of a 50 percent aqueous solution of sodium hydroxide added over a 15 minute period with stirring. This is followed by addition of 34.7 g (0.25 mole) 1-bromopentane over a period of 15 minutes and the reaction mixture allowed to stir for 3 hours. The reaction mixture is then extracted with diethyl ether which, after drying over magnesium sulfate, is evaporated. The resulting crude product is short-path distilled to obtain 2-(1-pentoxyethyl)furan in low yield (B.p. 35° C. at 0.2 mm Hg.). The structure of the 2-(1-pentoxyethyl)furan ##STR5## is confirmed by infrared and nuclear magnetic resonance spectroscopy.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04536349 |
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| Quelldatensatz | uspto-grants-1985_08 |
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| ORD ID | ord-19a8ea04c1314eceab388a6878981fce |
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| Quellennotiz | uspto-grants-1985_08 |
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