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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54271생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Trimethyltin chlorideHCID 14016—
반응물3-Methyl-3-(4-chlorophenyl)-1-iodo-1-buteneHCID 54263888—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물3-Methyl-3-(4-chlorophenyl)-1-trimethylstannyl-1-buteneHCID 6763290087.3%

반응 조건

온도-90 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05622954
출처 데이터셋uspto-grants-1997_04
ORD IDord-5265c609d750480b8b3ec7e1eb63a113
출처 메모uspto-grants-1997_04