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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 502861Erstellt: 27. Oktober 2026

Sodium Bicarbonate → 4-(beta-D-glucopyranos-1-yl)-2-(4-pentafluoroethyl-benzyl)-benzonitrile

https://huagongshe.com/reaction/502861

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
EduktPotassium FluorideHCID 522689—
Edukt(Pentafluoroethyl)trimethylsilaneHCID 2760820—
Edukt4-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranos-1-yl)-2-(4-iodo-benzyl)-benzonitrileHCID 86616250—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(beta-D-glucopyranos-1-yl)-2-(4-pentafluoroethyl-benzyl)-benzonitrileHCID 86616249—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A flask charged with 4-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranos-1-yl)-2-(4-iodo-benzyl)-benzonitrile (0.16 g), pentafluoroethyltrimethylsilane (0.14 g), KF (43 mg), CuI (0.16 g), DMF (2 mL) and Ar atmosphere is heated at 60° C. for 24 h. Then, aqueous NaHCO3 solution is added and the resulting mixture is extracted with ethyl acetate. The combined organic phases are dried over sodium sulfate and the solvent is removed. The residue is dissolved in methanol (8 mL) and treated with 4 M KOH solution (0.8 mL). The solution is stirred at room temperature for 1 h and then diluted with aqueous NaHCO3 solution. After removal of the methanol under reduced pressure, the residue is extracted with ethyl acetate, the combined organic extracts are dried and the solvent is removed. The residue is chromatographed on silica gel (dichloromethane/methanol 1:0->8:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07776830B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-4702331ee8d9449e95684ad0435736f6
Quellennotizuspto-grants-2010_08