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HRID 640827作成日:2026年10月27日

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

https://huagongshe.com/reaction/640827

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-Nitrobenzoyl chlorideHCID 8502—
反応物OxindoleHCID 321710—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物5-(4-Nitro-benzoyl)-1,3-dihydro-indol-2-oneHCID 6870071496%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07692005B2
出典データセットuspto-grants-2010_04
ORD IDord-3eff361f05ac4d189a169f420da34441
出典メモuspto-grants-2010_04