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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 355641Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSucroseHCID 5988—
Eduktethyl-(2R)-methyl-(3S)-hydroxybutanoateHCID 642623—
Eduktethyl (2S,3S)-3-hydroxy-2-methylbutanoateHCID 11789342—
KatalysatorDihydroxy(dioxo)molybdenum;phosphonic acidHCID 21863154—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelSulfuric AcidHCID 1118—
Produktethyl (2R,3S)-2-ethyl-3-hydroxybutyrateHCID 13215285—

Reaktionsbedingungen

Temperatur30 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05834261
Quelldatensatzuspto-grants-1998_11
ORD IDord-cac7673be92c4346afdbea1336040fb1
Quellennotizuspto-grants-1998_11