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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602939생성일: 2026년 10월 24일

Triethylamine → Triisopropyl{[4-(2,4,5-trifluorophenyl)cyclohex-1-en-1-yl]oxy}silane

https://huagongshe.com/ko/reaction/602939

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ammonium ChlorideHCID 25517—
반응물Triisopropylsilyl trifluoromethanesulfonateHCID 2724529—
반응물4-(2,4,5-Trifluorophenyl)cyclohexanoneHCID 57424362—
용매DichloromethaneHCID 6344—
생성물Triisopropyl{[4-(2,4,5-trifluorophenyl)cyclohex-1-en-1-yl]oxy}silaneHCID 67065786—

반응 조건

온도0 °C

반응 단계

A three-neck flask (1 L) containing a stirred solution of 4-(2,4,5-trifluorophenyl)cyclohexanone (15.8 g) in dichloromethane (160 mL) under a nitrogen atmosphere was cooled to 0° C. and then treated with triethylamine (22 mL) followed by triisopropylsilyl trifluoromethanesulfonate (25.4 g) while maintaining the temperature below 5° C. The solution was stirred at 0° for 30 min and then allowed to rise to ambient temperature over a period of 0.5 h. It was then treated with saturated aqueous ammonium chloride solution. The organic layer was separated, dried over anhydrous magnesium sulfate and evaporated. The crude product was chromatographed (silica gel, 3% ether in hexane) to yield the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906649B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-d4f395ba346b46dc933b09a0407c3940
출처 메모uspto-grants-2011_03