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HRID 6452作成日:2026年10月26日

Chlorotrimethylsilane → Cyclopentyl dimethoxy oxa-3-cyclopentyloxysilane

https://huagongshe.com/reaction/6452

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物3-Furanol, tetrahydro-HCID 9960—
反応物CyclopentyltrimethoxysilaneHCID 9855701—
触媒Sodium MethoxideHCID 10942334—
生成物Cyclopentyl dimethoxy oxa-3-cyclopentyloxysilaneHCID 1979381454%

反応手順

In a 100 ml three-neck flask provided with a magnetic stirrer and a reflux condenser were charged 7.7 g (0.0404 mole) of cyclopentyl trimethoxysilane, 35.7 g (0.405 mole) of 3-hydroxy tetrahydrofurane and 53.0 mg (0.98 m mole) of sodium methoxide, which were then reacted with each other in an oil bath of 80° C. for 2 hours under stirring. After cooled, trimethylchlorosilane was added to neutralize the alkali. Then, 5.37 g (0.0218 mole) of cyclopentyl dimethoxy oxa-3-cyclopentyloxysilane were obtained by vacuum distillation. Its structure was confirmed as in Example 1. The yield was 54%.

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-4f67e89866a749378b2de7b9b7e24fbf
出典メモuspto-grants-1993_09