HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dihydroxybenzaldehyde → 3-[(2,4-Dihydroxyphenyl)methylidene]-1,3-dihydro-2H-indol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dihydroxybenzaldehyde | HCID 7213 | — |
| Reactant | Indol-2-one | HCID 17904787 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[(2,4-Dihydroxyphenyl)methylidene]-1,3-dihydro-2H-indol-2-one | HCID 68616828 | — |
Reaction Steps
A mixture of 1.33 g of indole-2-one (10 mmol), 1.38 g of 2,4-dihydroxybenzaldehyde (10 mmol) and 3 drops of piperidine are refluxed in 40 ml of ethanol for 5 hours. The desired product precipitates as a yellow solid during the reaction. After cooling to room temperature, the product is filtered off, washed with ethanol and dried in vacuo. Yield 1.28 g (51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08324267B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-4fc6df65fb564f64aa648f8ec1e5e8c5 |
| Source note | uspto-grants-2012_12 |