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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9656Erstellt: 23. Oktober 2026

Tributyltin Chloride → Tributyl[5-(1,3-dioxolan-2-yl)4-methylthien-2-yl]stannane

https://huagongshe.com/de/reaction/9656

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributyltin ChlorideHCID 15096—
Edukt2-(3-Methylthiophen-2-yl)-1,3-dioxolaneHCID 12926522—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTributyl[5-(1,3-dioxolan-2-yl)4-methylthien-2-yl]stannaneHCID 21986287—

Reaktionsbedingungen

Temperatur-60 °C

Reaktionsschritte

A mixture of 2-(3-methylthien-2-yl)-1,3-dioxolane (intermediate 75, 1.5 g) in tetrahydrofuran (50 ml), stirred at −60° C. under a nitrogen atmosphere, was treated drop-wise with 1.6M n-butyl lithium in hexanes (6.1 ml). The reaction mixture was stirred at this temperature for 1 hour and tributyltin chloride (2.6 ml) was added; stirring was continued at −60° C. for 1 hour and then the reaction allowed to warm to ambient temperature. After 18 hours the reaction mixture was diluted with diethylether and this mixture was extracted with water and the ether layer dried with brine and over magnesium sulfate. The product isolated after evaporation of the solvent was further purified by flash column chromatography using cyclohexane:ethyl acetate (50:1) as eluent to give the title compound as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091237B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-bdd6a74b4fde4fe1a64ca556ea6560a2
Quellennotizuspto-grants-2006_08