Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Chlorotrimethylsilane → Cyclopentyl dimethoxy oxa-3-cyclopentyloxysilane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Chlorotrimethylsilane | HCID 6397 | — |
| 반응물 | 3-Furanol, tetrahydro- | HCID 9960 | — |
| 반응물 | Cyclopentyltrimethoxysilane | HCID 9855701 | — |
| 촉매 | Sodium Methoxide | HCID 10942334 | — |
| 생성물 | Cyclopentyl dimethoxy oxa-3-cyclopentyloxysilane | HCID 19793814 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05248803 |
| 출처 데이터셋 | uspto-grants-1993_09 |
| ORD ID | ord-4f67e89866a749378b2de7b9b7e24fbf |
| 출처 메모 | uspto-grants-1993_09 |