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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1839608생성일: 2026년 10월 24일

Acetic Acid → 4-(3-Bromo-phenyl)1,3-dihydro-indol-2-one

https://huagongshe.com/ko/reaction/1839608

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물PyridiniumtribromideHCID 21124087—
반응물4-(3-Bromo-phenyl)-1H-indoleHCID 22561906—
촉매ZincHCID 23994—
용매t-BuOH ethanol aceticacidHCID 86587657—
생성물4-(3-Bromo-phenyl)1,3-dihydro-indol-2-oneHCID 2256184965%

반응 조건

온도27 °C

반응 단계

To the suspension of 4-(3-bromo-phenyl)-1H-indole (1.48 g, 5.44 mmol) in t-BuOH-ethanol-acetic acid (3:2:1) (66 mL) was added pyridinium tribromide (90% purity from Aldrich, 5.80 g, 16.3 mmol)) portionwise. The mixture was stirred at 27° C. for 3 hours, and then to the mixture was added acetic acid (26 mL). Zinc dust was added to the reaction mixture portionwise until the color changed from deep red to light yellow, and the reaction mixture was stirred at room temperature for one hour. The unreacted zinc dust was filtered off and washed with ethanol. The filtrate was concentrated, and the syrupy residue was dissolved in ethyl acetate, which was washed with water, 0.5 N HCl, sat. NaHCO3 and brine, and dried over Na2SO4. After filtration and evaporation, the crude product was triturated with diethyl ether to provide product 4-(3-bromo-phenyl)-1,3-dihydro-indol-2-one (1.02 g, 65%) as a tan solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06677368B2
출처 데이터셋uspto-grants-2004_01
ORD IDord-caa3a5a453394d30ae087781c611797f
출처 메모uspto-grants-2004_01