戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1754034作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物MethaneHCID 297—
反応物1-HexanolHCID 8103—
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Butanoic acid, 2-hydroxy-4-(methylthio)-, hexyl esterHCID 10014278—

反応手順

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+).

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-1aa00c471ae14729b3732a9de8bc8fbe
出典メモuspto-grants-2015_10