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HRID 54271作成日:2026年10月23日

Water → 3-Methyl-3-(4-chlorophenyl)-1-trimethylstannyl-1-butene

https://huagongshe.com/ja/reaction/54271

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Trimethyltin chlorideHCID 14016—
反応物3-Methyl-3-(4-chlorophenyl)-1-iodo-1-buteneHCID 54263888—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物3-Methyl-3-(4-chlorophenyl)-1-trimethylstannyl-1-buteneHCID 6763290087.3%

反応条件

温度-90 °C

反応手順

A stirring solution of 4.8 grams (0.016 mole) of 3-methyl-3-(4-chlorophenyl)-1-iodo-1-butene in 50 mL of tetrahydrofuran is cooled to about -90° C., and 6.9 mL (0.01 8 mole) of n-butyllithium (2.5M in hexane) is added dropwise at a rate to maintain the reaction mixture temperature at about -85° to -90° C. Upon completion of the addition, the reaction mixture is stirred at -90° C. for 30 minutes. After this time, a solution of 3.7 grams (0.019 mole) of trimethyltin chloride in 10 mL of tetrahydrofuran is added dropwise at a rate sufficient to maintain the reaction mixture temperature at about -85° to -90° C. Upon completion of addition, the reaction mixture is again stirred at -90° C. for 30 minutes. After this time, the reaction mixture is allowed to warm to ambient temperature where it is stirred for about 18 hours. The reaction mixture is then poured into 150 mL of water and extracted with 150 mL of diethyl ether. The ether extract is dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure, yielding 4.8 grams of 3-methyl-3-(4-chlorophenyl)-1-trimethylstannyl-1-butene. The NMR spectrum is consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05622954
出典データセットuspto-grants-1997_04
ORD IDord-5265c609d750480b8b3ec7e1eb63a113
出典メモuspto-grants-1997_04