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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 495300Erstellt: 25. Oktober 2026

Tetrahydrofuran → Stannane, tributyl[5-(1,3-dioxolan-2-yl)-2-furanyl]-

https://huagongshe.com/reaction/495300

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktTributyltin ChlorideHCID 15096—
Edukt2-Furyl-1,3-dioxolaneHCID 263158—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelHexaneHCID 8058—
ProduktStannane, tributyl[5-(1,3-dioxolan-2-yl)-2-furanyl]-HCID 1096095275,5%

Reaktionsschritte

Tetrahydrofuran (10 mL) solution of 2-(1,3-dioxolan-2-yl)furan (1.0 g, 7.1 mmol) was cooled to −78° C., and n-hexane solution of 1.6 mol/L n-butyllithium (4.5 mL, 7.2 mmol) was dropwise added thereto, and stirred for 3 hours. Tributyltin chloride (2.6 g, 7.9 mmol) was dropwise added to the reaction mixture, and stirred for 5 hours with heating up to room temperature. Water (10 mL) was added to the reaction mixture, and extracted with ethyl acetate (50 mL). The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated away under reduced pressure. The resulting residue was purified through silica gel column chromatography (n-hexane to ethyl acetate/n-hexane=1/20) to obtain tributyl[5-(1,3-dioxolan-2-yl)furan-2-yl]tin (2.3 g, 75%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07538241B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-92705236b5794a5bb01450d143a7c481
Quellennotizuspto-grants-2009_05