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HRID 2106413作成日:2026年10月25日

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

https://huagongshe.com/reaction/2106413

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物5-Bromo-2-fluorobenzaldehydeHCID 736327—
反応物((4-Bromophenyl)ethynyl)triisopropylsilaneHCID 57809595—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物(5-Bromo-2-fluoro-phenyl)-{4-[(triisopropylsilyl)-ethynyl]-phenyl}methanolHCID 57809581—

反応条件

温度-78 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07579449B2
出典データセットuspto-grants-2009_08
ORD IDord-0cdab6fdac004177b7a929c51952fbf4
出典メモuspto-grants-2009_08