HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299603Generated: October 26, 2026
Pyruvic Acid → Potassium 2-oxo-8-phenyl-3,5,7-octatrienoate
https://huagongshe.com/reaction/2299603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyruvic Acid | HCID 1060 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,4-Pentadienal, 5-phenyl- | HCID 114651 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Potassium 2-oxo-8-phenyl-3,5,7-octatrienoate | HCID 74088932 | — |
Reaction Steps
A solution of 5-phenyl-2,4-pentadienal (6.70 g) and pyruvic acid (3.0 mL) in 5 mL of methanol was stirred and chilled to 0-5° C. in an ice bath. To the chilled solution was added a solution of 35 mL of potassium hydroxide (3.5 g) in 10 mL of methanol dropwise over a period of 30 minutes. The remaining methanolic potassium hydroxide was added rapidly and the ice bath was removed. The reaction was allowed to warm to room temperature and stirred for another hour. The flask was then refrigerated overnight. The solid was collected by filtration, washed with 15 mL of methanol three times, 15 mL of ether and then air dried to afford 6.69 g of potassium 2-oxo-8-phenyl-3,5,7-octatrienoate as a yellow solid. 1H NMR (DMSO-d6, 300 MHz), δ(ppm) 7.52 (d, 2H), 7.32 (m, 3H), 7.10 (m, 2H), 6.83 (dd, 2H), 6.57 (dd, 1H), 6.13 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06495719B2 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-391e9445a36043059cadadf971b8b14e |
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| Source note | uspto-grants-2002_12 |
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