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HRID 434395作成日:2026年10月27日

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

https://huagongshe.com/reaction/434395

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物ChlorotrimethylsilaneHCID 6397—
反応物1-Bromo-4-((trimethylsilyl)oxy)benzeneHCID 87350—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物Trimethyl{4-[(trimethylsilyl)oxy]phenyl}silaneHCID 26289060.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04396704
出典データセットuspto-grants-1983_08
ORD IDord-c978f15b4ae14abdb51962b800d2cbd6
出典メモuspto-grants-1983_08