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HRID 6450作成日:2026年10月23日

Chlorotrimethylsilane → Cyclopentyloxy cyclopentyl dimethoxysilane

https://huagongshe.com/ja/reaction/6450

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物CyclopentanolHCID 7298—
反応物CyclopentyltrimethoxysilaneHCID 9855701—
触媒Sodium MethoxideHCID 10942334—
生成物Cyclopentyloxy cyclopentyl dimethoxysilaneHCID 1979381585.1%

反応手順

In a 50 ml three-neck flask provided with a magnetic stirrer and a reflux condenser were charged 5.0 g (0.0262 mole) of cyclopentyl trimethoxysilane, 22.5 g (0.262 mole) of cyclopentyl alcohol and 18.6 mg (0.34 m mole) of sodium methoxide, which were then reacted with each other at room temperature for 2 hours under stirring. Then, trimethylchlorosilane was added to neutralize the alkali. Then, 5.4 g (0.0223 mole) of cyclopentyloxy cyclopentyl dimethoxysilane were obtained by vacuum distillation. Its structure was confirmed as in Example 1. The yield was 85%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05248803
出典データセットuspto-grants-1993_09
ORD IDord-26d59802162f454b919e6a3c67915737
出典メモuspto-grants-1993_09