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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6452생성일: 2026년 10월 25일

Chlorotrimethylsilane → Cyclopentyl dimethoxy oxa-3-cyclopentyloxysilane

https://huagongshe.com/reaction/6452

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물3-Furanol, tetrahydro-HCID 9960—
반응물CyclopentyltrimethoxysilaneHCID 9855701—
촉매Sodium MethoxideHCID 10942334—
생성물Cyclopentyl dimethoxy oxa-3-cyclopentyloxysilaneHCID 1979381454%

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248803
출처 데이터셋uspto-grants-1993_09
ORD IDord-4f67e89866a749378b2de7b9b7e24fbf
출처 메모uspto-grants-1993_09