HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Indanone → Benzoic acid, 4-[(1,3-dihydro-1-oxo-2H-inden-2-ylidene)methyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Indanone | HCID 6735 | — |
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Benzoic acid, 4-[(1,3-dihydro-1-oxo-2H-inden-2-ylidene)methyl]- | HCID 5033086 | 68.2% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a suspension of indanone (2.00 g, 15.1 mmol) and 4-carboxybenzaldehyde (1.89 g, 12.6 mmol) in EtOH (10 ml) was added KOH (1.77 g, 31.5 mmol) at 0° C. The reaction mixture was stirred 30 min at 0° C. then at room temperature for 16 h. The solvent was evaporated and the residue was dissolved in water, acidified to pH 5 with HCl 1 M. The precipitate was filtered and rinsed with water to afford the title compound 273 (2.27 g, 57%) as a yellow solid. LRMS: 264.1 (Calc.); 265.0 (found).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07868204B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-a4a454e2cb844ce89b933c191d2b8fea |
| Source note | uspto-grants-2011_01 |