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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 434395생성일: 2026년 10월 26일

Methyl iodide → Trimethyl{4-[(trimethylsilyl)oxy]phenyl}silane

https://huagongshe.com/reaction/434395

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물ChlorotrimethylsilaneHCID 6397—
반응물1-Bromo-4-((trimethylsilyl)oxy)benzeneHCID 87350—
반응물MagnesiumHCID 5462224—
용매TetrahydrofuranHCID 8028—
생성물Trimethyl{4-[(trimethylsilyl)oxy]phenyl}silaneHCID 26289060.2%

반응 단계

5.35 g (0.22 mole) magnesium was added to 10 ml tetrahydrofuran and 0.35 ml CH3I under N2 and heated to initiate the Grignard reaction. A solution of 49.0 g (0.2 mole) p-bromophenyoxytrimethylsilane and 63 ml tetrahydrofuran was added over a 11/2 hour period. The reaction mixture was refluxed one additional hour and then cooled to room temperature. 22.8 g (0.21 mole) chlorotrimethylsilane was added to the reaction mixture. Once again the mixture was refluxed 1 hour and then cooled. 100 ml distilled water was slowly added, stirred, and separated. The organic phase was washed with two 50 ml portions of water and finally 50 ml of brine. The organic solution was dried over magnesium sulfate, filtered, and the solvent removed on a rotary evaporator under reduced pressure. Vacuum distillation gave 28.7 g of p-trimethylsilylphenoxytrimethylsilane, bp 132 degrees Celsius at 27 mm Hg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04396704
출처 데이터셋uspto-grants-1983_08
ORD IDord-c978f15b4ae14abdb51962b800d2cbd6
출처 메모uspto-grants-1983_08