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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 268650생성일: 2026년 10월 25일

Lithium borohydride → 5-bromo-7-ethyl-1H-indole

https://huagongshe.com/reaction/268650

반응식

참여 물질

역할이름HCID투입량
반응물Lithium borohydrideHCID 4148881—
반응물5-Bromo-7-ethylindoline-2,3-dioneHCID 8033813—
용매TetrahydrofuranHCID 8028—
생성물5-bromo-7-ethyl-1H-indoleHCID 21071575—

반응 조건

온도90 °C

반응 단계

To a solution of 5-bromo-7-ethyl-1H-indole-2,3-dione (36.g, 144 mmol) in tetrahydrofuran (120 mL) at room temperature was dropped a 2.0 M solution of lithium borohydride in tetrahydrofuran. The reaction mixture was stirred at 90° C. (oil bath) for 5 hours. After cooling down to room temperature, it was quenched with 5% hydrochloric acid solution until the excess lithium borohydride was destroyed. To the mixture was added saturated sodium bicarbonate solution (300 mL) and extracted with ethyl acetate. Extracts were dried over magnesium sulfate and concentrated under reduced pressure to give the crude product of 5-bromo-7-ethyl-1H-indole, which went to next reaction without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07446122B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-2f4bbbd98ec54a318d290e8cac149fe1
출처 메모uspto-grants-2008_11