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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2352765생성일: 2026년 10월 26일

Hydrochloric Acid → 5-(4-Nitro-benzoyl)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/2352765

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Nitrobenzoyl chlorideHCID 8502—
반응물OxindoleHCID 321710—
반응물Aluminum(III) ChlorideHCID 6451240—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물5-(4-Nitro-benzoyl)-1,3-dihydro-indol-2-oneHCID 6870071496%

반응 단계

AlCl3 (20.0 g, 150 mmol) was placed in a dry 200 mL round bottom flask and DMF (3.30 mL) was added dropwise at 0° C. During the addition of DMF care was taken to ensure that the reaction was allowed to vent to the outside as this addition caused an exotherm to occur. Additionally as the DMF was added a white suspension formed. This suspension was allowed to stir for 30 min at room temperature, after which 4-nitrobenzoyl chloride (2.984 g, 16 mmol) was added. The mixture was warmed to 50° C. and stirred for 15 min at that temperature. The 50° C. mixture then was treated with oxindole (2.051 g, 15 mmol). The resulting reaction mixture was heated to 90° C. and allowed to stir for 5 hours during which the reaction mixture turned from a yellowish suspension to a thick black oil. The reaction was cooled to room temperature. Ice was added directly to the flask followed by water, turning the black oil into a pale yellow/white precipitate. Concentrated HCl(aq) (3 mL) was added to the reaction and the contents were stirred at room temperature for 15 min. The precipitate was collected via vacuum filtration. The crude solid was purified by washing with sat. NaHCO3(aq) providing 5-(4-Nitro-benzoyl)-1,3-dihydro-indol-2-one as a gray solid (4.05 g, 14.4 mmol, 95%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07749530B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-d2348a7ac914442798744accf77cbf5f
출처 메모uspto-grants-2010_07