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HRID 1754041作成日:2026年10月24日

Methane → Octadecyl 2-hydroxy-4-(methylthio)butanoate

https://huagongshe.com/ja/reaction/1754041

反応式

関与物質

役割名称HCID仕込み量
反応物MethaneHCID 297—
反応物Stearyl AlcoholHCID 8221—
反応物alpha-Hydroxy-gamma-methylmercaptobutyric acidHCID 11427—
反応物Sodium BisulfateHCID 516919—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物Octadecyl 2-hydroxy-4-(methylthio)butanoateHCID 86689973—

反応手順

To a 3 neck 3 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 (130 g, 870 mmol, obtained by stirring Alimet over activated charcoal, filtering and concentrating in a rotovap), 1-octadecanol (351.2 g, 1.30 mol), sodium hydrogen sulfate (2.10 g, 17 mmol), and toluene (1000 mL). The reaction was heated to reflux with removal of water (21.5 mL) during the course of about 4 hours. The reaction was cooled to room temperature overnight and the mixture was filtered. The filtrate was washed with saturated NaHCO3 (1×500 mL), DI water (1×500 mL) and brine (1×500 mL), dried over sodium sulfate, filtered and evaporated to give light brown semi-solid (319.4 g). The semi-solid was treated with hexanes (750 mL) and the resulting mixture was filtered. The solid was washed with hexanes (250 mL) and the combined filtrate was evaporated to give an oil which solidified upon standing (278.8 g). The solid was purified by kugelrohr at 175° C. and 0.1 mm Hg vacuum to give a waxy solid remaining in the distillation pot (214.0 g, 61%). m/z 425 (MNa+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09169203B2
出典データセットuspto-grants-2015_10
ORD IDord-aff56a75d5bf4fa4a032f5ad9d629bad
出典メモuspto-grants-2015_10