HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 2-Benzylidene-1,3-indandione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 1,3-Indandione | HCID 11815 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Benzylidene-1,3-indandione | HCID 237822 | 72.1% |
Reaction Steps
To a solution of 1,3-indandione (43.8 g) and piperidine (44 mg) in dry benzene (500 ml) was added benzaldhyde (31.8 g). The mixture was heated to reflux and the water generated was removed by Dean-Stark trap. After 24 hours, the mixture was evaporated to dryness. The residue was recrystallized from ethanol (200 ml) to give 2-benzylidene-1,3-indandione as a yellow solid (50.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06153645 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-4cdc2d56b9d643e9bb22b4106b8ec394 |
| Source note | uspto-grants-2000_11 |