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HRID 355641作成日:2026年10月24日

Sucrose → ethyl (2R,3S)-2-ethyl-3-hydroxybutyrate

https://huagongshe.com/ja/reaction/355641

反応式

関与物質

役割名称HCID仕込み量
反応物SucroseHCID 5988—
反応物ethyl-(2R)-methyl-(3S)-hydroxybutanoateHCID 642623—
反応物ethyl (2S,3S)-3-hydroxy-2-methylbutanoateHCID 11789342—
触媒Dihydroxy(dioxo)molybdenum;phosphonic acidHCID 21863154—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Sulfuric AcidHCID 1118—
生成物ethyl (2R,3S)-2-ethyl-3-hydroxybutyrateHCID 13215285—

反応条件

温度30 °C

反応手順

Twenty grams of bakers' yeast (Sigma Chemical Company, Saccharomyces cerevisiae, type II) was suspended in a solution of 30 grams of sucrose in water in a conical flask, and the mixture was placed in an orbital shaker chamber maintained at 220 rpm and 30° C. for 30 minutes to initiate fermentation. Two grams of ethyl 2-ethyl acetoacetate was dissolved in 2 ml of 95% ethanol, the resulting solution was added to the fermenting yeast, and shaking was resumed. The reaction was followed by TLC (staining with phosphomolybdic acid in ethanolic sulfuric acid) to monitor the consumption of starting material and the production of product alcohol. After approximately 48 hours the reaction was judged complete, and the reaction was terminated by removing the flask from the shaker and adding 20-30 grams of Celite to the reaction mixture. The resulting suspension was suction filtered through a pad of Celite, and the clear yellow filtrate was extracted with ethyl acetate (4×200 ml). The extracts were combined, dried over MgSO4, filtered, and rotary evaporated to leave 1.6 grams of a yellowish oil containing ethyl (2R,3S)-2-methyl-3-hydroxybutyrate as the major product (80%) and ethyl (2S,3S)-2-methyl-3-hydroxybutyrate (20%) as the minor product as judged by chiral chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05834261
出典データセットuspto-grants-1998_11
ORD IDord-cac7673be92c4346afdbea1336040fb1
出典メモuspto-grants-1998_11