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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1840491Erstellt: 26. Oktober 2026

Indole-2-carboxaldehyde → 3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-carboxylic acid

https://huagongshe.com/reaction/1840491

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIndole-2-carboxaldehydeHCID 96389—
Edukt2-Oxindole-5-carboxylic acidHCID 2773318—
KatalysatorPiperidineHCID 8082—
LösungsmittelEthanolHCID 702—
Produkt3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-carboxylic acidHCID 5409037040%

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

A mixture of 5-carboxy-2-oxindole (88.5 mg) (prepared as described in Compound IN-05), indole-2-carbaldehyde (87 mg) (prepared according to Synthetic Communications, 1993, 23, 3109) and piperidine (1 drop) in ethanol (3 mL) was heated in a sealed tube at 95° C. for 4 hours. The mixture was cooled to room temperature. The solid was filtered and acidified with 2N hydrochloric acid. The resulting darker solid was collected by vacuum filtration, washed with cold ethanol and dried in vacuum oven for overnight to give 60 mg (40% yield) of 3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-carboxylic acid as a mustard-colored solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06680335B2
Quelldatensatzuspto-grants-2004_01
ORD IDord-c97db97c0d9b49a784ee8ca5880e5230
Quellennotizuspto-grants-2004_01