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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2352765Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2352765

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-Nitrobenzoyl chlorideHCID 8502—
EduktOxindoleHCID 321710—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-(4-Nitro-benzoyl)-1,3-dihydro-indol-2-oneHCID 6870071496%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07749530B2
Quelldatensatzuspto-grants-2010_07
ORD IDord-d2348a7ac914442798744accf77cbf5f
Quellennotizuspto-grants-2010_07