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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1029378생성일: 2026년 10월 26일

3,3,3-Trifluoropropyl-trimethoxysilane → 3,3,3-Trifluoropropyl(isobutyl)dimethoxy silane

https://huagongshe.com/reaction/1029378

반응식

참여 물질

역할이름HCID투입량
반응물3,3,3-Trifluoropropyl-trimethoxysilaneHCID 67933—
반응물Silane hexaneHCID 131717238—
반응물HCID 178418368HCID 178418368—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물3,3,3-Trifluoropropyl(isobutyl)dimethoxy silaneHCID 19900042—

반응 단계

Under nitrogen, a 500 ml Schlenk flask was cooled to room temperature and charged with 150 ml of diethyl ether and isobutylmagnesium chloride (0.06 mol, 30.24 ml). This was stirred and heated slightly to 30° C. A second Schlenk flask (100 ml) was purged with nitrogen to room temperature and charged with 75 ml hexane and 3,3,3-trifluoropropyltrimethoxy silane (0.0504 mol, 10 ml) and stirred. The silane/hexane solution was added dropwise via cannula to the Grignard/diethyl ether mixture producing a white precipitate midway through the addition. After addition (1.25 hrs.), the reaction mixture was stirred at room temperature for one hour. The flask was fitted with a reflux condenser and the reaction mixture was refluxed for two hours, then allowed to cool to room temperature. The reaction mixture was filtered through a medium porosity frit, using Celite diatomaceous earth and glass wool as a filtering aid. The solids collected weighed 7.55 g (theoretical=4.56 grams of magnesium salts). The slightly cloudy filtrate was kept under nitrogen overnight.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05102842
출처 데이터셋uspto-grants-1992_04
ORD IDord-25c09710342543ffa93dee71783fd183
출처 메모uspto-grants-1992_04