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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1835728Erstellt: 25. Oktober 2026

Sodium hydride → HCID 54432354, Verbindung

https://huagongshe.com/reaction/1835728

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt8-Bromo-3,7-dimethyl-3,7-dihydro-1H-purine-2,6-dioneHCID 702242—
Edukt(R)-5-acetoxyhexyl-1-chlorohexaneHCID 86584512—
LösungsmittelDimethyl SulfoxideHCID 679—
ProduktHCID 54432354HCID 5443235474%

Reaktionsschritte

To a stirring suspension of sodium hydride (740 mg, 30.8 mmol) in anhydrous dimethylsulfoxide (120 ml) was added 8-bromo-3,7-dimethylxanthine (6.5 g, 25.0 mmol). After stirring at room temperature under argon for 1.5 hours, (R)-5-acetoxyhexyl-1-chlorohexane (4.91 g, 27.5 mmol) was added and the mixture was stirred at 80° C. for 18 hours. After cooling to room temperature, the reaction mixture was quenched by addition of saturated aqueous sodium chloride solution (300 ml) and extracted with ethyl acetate (3×50 ml). The combined extracts were washed with water (2×20 ml), with saturated aqueous sodium chloride solution (20 ml) and dried over magnesium sulfate. After evaporation of the solvent under reduced pressure, the crude product was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:1) to provide (R)-1-(5-acetoxyhexyl)-8-bromo-3,7-dimethylxanthine (7.38 g, 74% yield) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06774130B2
Quelldatensatzuspto-grants-2004_08
ORD IDord-9afeedc4dc6c4fef8cfb30d24d794437
Quellennotizuspto-grants-2004_08