Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Bromide | HCID 6332 | — |
| Edukt | Malonic acid, disodium salt | HCID 8865 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | tert-Butyl methyl ether | HCID 15413 | — |
| Katalysator | Tetrabutylammonium Bromide | HCID 74236 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Diethyl Malonate | HCID 7761 | 45% |
Reaktionsschritte
In an autoclave, 10.9 g (0.1 mol) of ethyl bromide were added to a solution of 2.96 g (20 mmol) of disodium malonate and 0.64 g (2 mmol) of tetrabutylammonium bromide in 5 ml of water and 10 ml of tert-butyl methyl ether. The mixture was heated to 100° C. over a period of 30 minutes, with the pressure in the autoclave rising to 3.5 bar. After a reaction time of 3½ hours at 100° C., the mixture was cooled to room temperature and depressurized. The aqueous phase was brought from pH 4.2 to pH 5.5 using 1 M sodium hydroxide solution and extracted with tert-butyl methyl ether (2×5 ml). The combined organic phases were dried over sodium sulfate and analyzed by gas chromatography (internal standard: dimethyl succinate). The product yield was 45 percent.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06350898B1 |
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| Quelldatensatz | uspto-grants-2002_02 |
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| ORD ID | ord-97601e19138c4f28a6fa58d6a537c536 |
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| Quellennotiz | uspto-grants-2002_02 |
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