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HRID 9656作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Tributyltin ChlorideHCID 15096—
反応物2-(3-Methylthiophen-2-yl)-1,3-dioxolaneHCID 12926522—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Tributyl[5-(1,3-dioxolan-2-yl)4-methylthien-2-yl]stannaneHCID 21986287—

反応条件

温度-60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091237B2
出典データセットuspto-grants-2006_08
ORD IDord-bdd6a74b4fde4fe1a64ca556ea6560a2
出典メモuspto-grants-2006_08