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HRID 24039作成日:2026年10月23日

Water → 5-Bromo-1-(triisopropylsilyl)-1H-indole

https://huagongshe.com/ja/reaction/24039

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-BromoindoleHCID 24905—
反応物Triisopropylsilyl chlorideHCID 139400—
反応物Lithium bis(trimethylsilyl)amideHCID 57426343—
溶媒TetrahydrofuranHCID 8028—
生成物5-Bromo-1-(triisopropylsilyl)-1H-indoleHCID 279465292%

反応手順

Lithium hexamethyldisilazane [1.0 M] (44.7 mL, 44.4 mmol) was added to a solution of 5-bromo-1H-indole (7.30 g, 37.0 mmol) in tetrahydrofuran (50 mL) at room temperature. After stirring for 5 minutes, triisopropylsilyl chloride (8.62 g, 44.4 mmol) was added to reaction mixture and stirred for 30 minutes. Water was added to quench the reaction and the solvent was removed under reduced pressure to give the crude mixture, which was purified via column chromatography on silica gel (9:1 Hexane/ethyl acetate) to give the title compound in 92% yield. 1H NMR (CDCl3) δ 7.74 (d, J=1.8, 1H), 7.36 (d, J=8.8 Hz, 1H), 7.22 (m, 2H), 6.55 (d, J=3.1 Hz, 1H), 1.65 (m, 3H), 1.12 (d, J=7.5 Hz, 18H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855722B2
出典データセットuspto-grants-2005_02
ORD IDord-0561702af9fa4419aaedbad71faaa47d
出典メモuspto-grants-2005_02