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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840491Generated: October 25, 2026

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

https://huagongshe.com/reaction/1840491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndole-2-carboxaldehydeHCID 96389—
Reactant2-Oxindole-5-carboxylic acidHCID 2773318—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
Product3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-carboxylic acidHCID 5409037040%

Reaction Conditions

Temperature95 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680335B2
Source datasetuspto-grants-2004_01
ORD IDord-c97db97c0d9b49a784ee8ca5880e5230
Source noteuspto-grants-2004_01