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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49344생성일: 2026년 10월 25일

Triethylamine → [(e)-5-(4-Bromo-2-thienyl)-1,1-diethylhept-4-enyloxy]triethylsilane

https://huagongshe.com/reaction/49344

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-DimethylaminopyridineHCID 21885—
반응물Triethylsilyl trifluoromethanesulphonateHCID 2733308—
반응물(e)-7-(4-Bromo-2-thienyl)-3-ethylnon-6-en-3-olHCID 69824523—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물[(e)-5-(4-Bromo-2-thienyl)-1,1-diethylhept-4-enyloxy]triethylsilaneHCID 69825241—

반응 조건

온도0 °C

반응 단계

11.8 g (35.6 mmol) of (E)-7-(4-bromo-2-thienyl)-3-ethylnon-6-en-3-ol are dissolved in 150 mL of dichloromethane. 130 mg (1.1 mmol) of dimethylaminopyridine and 14.9 mL (107 mmol) of triethylamine are added. The reaction medium is cooled to 0° C. and 12.1 mL (53.4 mmol) of triethylsilyl trifluoromethanesulphonate are added dropwise. The medium is warmed to room temperature and stirred for 15 minutes, after which it is poured into 150 mL of water and extracted with dichloromethane. After chromatography on silica gel (eluent: heptane), the desired product is obtained in the form of a colourless oil (m=15 g; Y=100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706725B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-61c3221b133044d69ab1c621e42a83c4
출처 메모uspto-grants-2004_03