Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methane | HCID 297 | — |
| Edukt | 1-Decanol | HCID 8174 | — |
| Edukt | alpha-Hydroxy-gamma-methylmercaptobutyric acid | HCID 11427 | — |
| Edukt | Sodium Bisulfate | HCID 516919 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | Decyl 2-hydroxy-4-(methylthio)butanoate | HCID 86689969 | — |
Reaktionsschritte
To a 4 neck 1 L round bottom flask fitted with a reflux condenser, dean stark trap, thermocouple, and mechanical overhead stirrer was added 2-hydroxy-4-(methylthio)butanoic acid (125 g, 832.2 mmol, obtained for example by stirring Alimet over activated charcoal, filtering and concentrating in a rotovap), 1-decanol (238 mL, 1248 mmol), sodium hydrogen sulfate (1.998 g, 16.64 mmol), and toluene (625 mL). The reaction was heated to reflux with removal of water (16 mL) during the course of about 6 hours and the reaction was monitored by GC analysis. The reaction was cooled to room temperature overnight and the organic layer was washed with saturated NaHCO3 (1×300 mL), DI water (1×300 mL) and brine (2×300 mL), dried over sodium sulfate, filtered and evaporated to give an amber oil (395.5 g). The oil was purified by kugelrohr distillation at 110° C. and 0.1 Torr vacuum to give an oil (105.23 g, 43.5%). m/z 313 (MNa+);
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09169203B2 |
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| Quelldatensatz | uspto-grants-2015_10 |
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| ORD ID | ord-0a6b743a53924e59a801996449794828 |
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| Quellennotiz | uspto-grants-2015_10 |
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