Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 2-Pentanone | HCID 7895 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 227280 | HCID 227280 | 79.7% |
Reaction Steps
To a mixture of benzaldehyde (30.00 g, 0.283 mole) and 2-pentanone (67.33 g, 0.782 mole) was added 10% aqueous sodium hydroxide (40.00 g, 0.10 mole) and the mixture was heated and stirred at 55-65° C. for 10 hr. The reaction mixture was cooled to room temperature and the aqueous layer was once separated. 5% Brine (20 g) was added and after stirring, the aqueous layer was separated. This step was repeated twice. The low boiling point content such as 2-pentanone, benzaldehyde and the like in the obtained organic layer were distilled away under reduced pressure to give the title compound as a pale-yellow green oil (138-150° C./1.33 kPa). (39.25 g, yield 79.7%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07038075B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-0c7a76ba45aa4a269e6a339ba812efce |
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| Source note | uspto-grants-2006_05 |
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