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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 617750생성일: 2026년 10월 26일

Indole → 1H-Indole, 3-bromo-1-[(1,1-dimethylethyl)dimethylsilyl]-

https://huagongshe.com/reaction/617750

반응식

참여 물질

역할이름HCID투입량
반응물IndoleHCID 798—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물N-bromobutanimideHCID 67184—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Hexane pyridineHCID 19761730—
생성물1H-Indole, 3-bromo-1-[(1,1-dimethylethyl)dimethylsilyl]-HCID 1024487580.6%

반응 단계

To a cold (-78°) solution of indole (4.0 g, 34 mmol) in THF (120 mL) was added nBuLi (2.5M/Hexanes) over 5 minutes. The solution was warmed to -10° (ice/salt bath) for 15 minutes, re-cooled to -78° and TBDMS-Cl (5.8 g, 38 mmol) was added in THF (30 mL). The solution was held at 0° for 3 hours, cooled to -78° and N-Bromosuccinimide (6.0 g, 34 mmol) was added in one portion. The solution was stirred coldfor 2 hours and then was allowed to warm to ambient temperature at which time hexane/pyridine (100 mL) was added to the solution and the resulting suspension was filtered over Celite. The organics were evaporated and the residue quickly purified by flash chromatography (hexanes/methylene chloride 2:1) giving 8.5 g of the desired compound as a slightly purple solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05952320
출처 데이터셋uspto-grants-1999_09
ORD IDord-405b71d3674d4db98015a12cf13a547a
출처 메모uspto-grants-1999_09