Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Acetyl chloride | HCID 6367 | — |
| Edukt | 1,3-Dioxolane | HCID 12586 | — |
| Katalysator | ZINC;ethoxyethane;dichloride | HCID 162251561 | — |
| Produkt | Acetic acid 2-chloromethoxy-ethyl ester | HCID 10034810 | — |
Reaktionsschritte
A 5 L three-neck flask was fitted with mechanical stirrer, thermometer, 500 mL additional funnel and argon purged. 1,3-Dioxalane (140 mL, 2.00 mol) in anhydrous Et2O (800 mL) and 1.0 M ZnCl2/Et2O (7.5 mL, 0.007 mol) were added. A solution of acetyl chloride (157 mL, 2.20 mol) in Et2O (200 mL) was added dropwise through an additional funnel over 20 min. A cold water bath was used to maintain temperature between 19-27° C. throughout. Continue stirring without external cooling for 4 h, reaction self heating at 20-25° C. for about 1 h. A clear, colorless solution retained under argon overnight. Stood for 3 days and formed an orange solution. Strip Et2O on rotavap (water aspirator) until no more distilled at 35° C. bath. A quantitative yield of product 318 g (theoretical yield 306 g) was obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08088754B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-39015a4064ef4bb1a13c9346652564d3 |
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| Quellennotiz | uspto-grants-2012_01 |
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