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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2106413생성일: 2026년 10월 24일

Water → (5-Bromo-2-fluoro-phenyl)-{4-[(triisopropylsilyl)-ethynyl]-phenyl}methanol

https://huagongshe.com/ko/reaction/2106413

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물5-Bromo-2-fluorobenzaldehydeHCID 736327—
반응물((4-Bromophenyl)ethynyl)triisopropylsilaneHCID 57809595—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물(5-Bromo-2-fluoro-phenyl)-{4-[(triisopropylsilyl)-ethynyl]-phenyl}methanolHCID 57809581—

반응 조건

온도-78 °C

반응 단계

33.8 ml of a 1.6 M solution of n-butyllithium in hexane are added dropwise under argon to a solution of 17.4 g 1-bromo-4-triisopropylsilylethynyl-benzene in 120 ml dry tetrahydrofuran chilled to −78° C. The solution is stirred for 1 h at −70° C. Then 10.8 g 5-bromo-2-fluoro-benzaldehyde dissolved in 30 ml of tetrahydrofuran are added dropwise over 15 min. The resulting solution is left in the cooling bath to warm up overnight to ambient temperature. Then water is added and the mixture is extracted with ethyl acetate. The combined organic phase are dried over sodium sulphate, and the solvent is removed. The residue is purified through silica gel (cyclohexane/ethyl acetate 4:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07579449B2
출처 데이터셋uspto-grants-2009_08
ORD IDord-0cdab6fdac004177b7a929c51952fbf4
출처 메모uspto-grants-2009_08