HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Fluoro-p-anisaldehyde → HCID 68617947, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Fluoro-p-anisaldehyde | HCID 67696 | — |
| Reactant | Indol-2-one | HCID 17904787 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68617947 | HCID 68617947 | — |
Reaction Steps
A mixture of 1.33 g of indole-2-one (10 mmol), 1.54 g of 3-fluoro-4-methoxybenzaldehyde (10 mmol) and 3 drops of piperidine are refluxed in 40 ml of ethanol for 5 hours. The desired product precipitates as a yellow crystalline solid during the reaction. After cooling to room temperature, the product is filtered off, washed with ethanol and dried in vacuo. Yield 2.2 g (82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08324267B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-5c232a12e65d488099c79f5e63dbb933 |
| Source note | uspto-grants-2012_12 |