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HRID 2246490作成日:2026年10月27日

Water → (3-Bromo-4-methoxy-phenyl)-{4-[(triisopropylsilyl)-ethynyl]-phenyl}-methanol

https://huagongshe.com/reaction/2246490

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物3-Bromo-4-methoxybenzaldehydeHCID 98662—
反応物((4-Bromophenyl)ethynyl)triisopropylsilaneHCID 57809595—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物(3-Bromo-4-methoxy-phenyl)-{4-[(triisopropylsilyl)-ethynyl]-phenyl}-methanolHCID 59217793—

反応条件

温度-78 °C

反応手順

14.8 mL of a 1.6 M solution of n-butyllithium in hexane are added dropwise under argon to a solution of 8.0 g 1-bromo-4-triisopropylsilylethynyl-benzene in 80 mL dry tetrahydrofuran chilled to −78° C. The solution is stirred for 1 h at −70° C. Then 5.1 g 3-bromo-4-methoxy-benzaldehyde dissolved in 20 mL tetrahydrofuran are added dropwise over 15 min. The resulting solution is left in the cooling bath to warm to ambient temperature overnight. Then water is added and the mixture is extracted with ethyl acetate. The combined organic phases are dried over sodium sulfate and the solvent is removed. The residue is purified over silica gel (cyclohexane/ethyl acetate 9:1->1:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07687469B2
出典データセットuspto-grants-2010_03
ORD IDord-c585e4de99e748a285166be8d639f9b9
出典メモuspto-grants-2010_03