戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 21909作成日:2026年10月24日

Tetrahydrofuran → Stannane, tributyl-3-furanyl-

https://huagongshe.com/ja/reaction/21909

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Tributyltin ChlorideHCID 15096—
反応物3-BromofuranHCID 89164—
反応物ButyllithiumHCID 178418339—
溶媒HexaneHCID 8058—
生成物Stannane, tributyl-3-furanyl-HCID 11760097—

反応条件

温度-60 °C

反応手順

69.5 ml of a 1.6 molar solution of n-butyllithium in hexane are mixed with 60 ml of absolute tetrahydrofuran. The mixture is cooled to -60° C. and 10 ml of 3-bromofuran are added dropwise at such a rate that the internal temperature does not exceed -50° C.. When the addition is complete, the whole is stirred for 15 minutes at -60° C. and then 33.2 ml of tributyltin chloride are added dropwise, during the course of which the internal temperature is not allowed to exceed -50° C.. When the addition is complete, the reaction solution is allowed to come to -10° C. and is then stirred for one hour at that temperature. The solution is then carefully quenched with water. The aqueous phase is extracted with ethyl acetate. The organic phase is washed with saturated sodium chloride solution and dried over sodium sulphate. It is filtered off and the solvent is removed in vacuo. The crude product obtained is purified by distillation in a high vacuum. 30.14 g of (3-furanyl)tributylstannane are obtained in the form of a light-yellow oil (boiling point=100°-104° C. at 0.09 torr).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05426102
出典データセットuspto-grants-1995_06
ORD IDord-6be063efd36f4a1c8d76b87968f64262
出典メモuspto-grants-1995_06