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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Indole-2-carboxaldehyde | HCID 96389 | — |
| Reactant | 2-Oxindole-5-carboxylic acid | HCID 2773318 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-carboxylic acid | HCID 54090370 | 40% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06680335B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-c97db97c0d9b49a784ee8ca5880e5230 |
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| Source note | uspto-grants-2004_01 |
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