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HRID 1754034Erstellt: 24. Oktober 2026

Methane → Butanoic acid, 2-hydroxy-4-(methylthio)-, hexyl ester

https://huagongshe.com/de/reaction/1754034

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethaneHCID 297—
Edukt1-HexanolHCID 8103—
Eduktalpha-Hydroxy-gamma-methylmercaptobutyric acidHCID 11427—
EduktSodium BisulfateHCID 516919—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
ProduktButanoic acid, 2-hydroxy-4-(methylthio)-, hexyl esterHCID 10014278—

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 (100 g, 666 mmol, obtained for example by stirring Alimet over activated charcoal, filtering and concentrating in a rotovap), 1-hexanol (125.4 mL, 999 mmol), sodium hydrogen sulfate (1.60 g, 13.32 mmol), and toluene (500 mL). The reaction was heated to reflux with removal of water (20 mL) during the course of about 5.5 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 (1×250 mL), DI water (1×250 mL) and brine (2×250 mL), dried over sodium sulfate, filtered and evaporated to give a brown oil (253.3 g). The oil was purified by kugelrohr distillation at 100° C. and 0.1 Torr vacuum to give a colorless oil (100.0 g, 64.1%). m/z 257 (MNa+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09169203B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-1aa00c471ae14729b3732a9de8bc8fbe
Quellennotizuspto-grants-2015_10