HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (E)-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzylidenepyruvic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(5-Methyl-2-phenyl-4-oxazolyl)methoxybenzaldehyde | HCID 10756116 | — |
| Reactant | Sodium pyruvate | HCID 23662274 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (E)-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzylidenepyruvic acid | HCID 18546125 | 44.5% |
Reaction Steps
A mixture of 4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzaldehyde (2.9 g), sodium pyruvate (3.3 g), sodium carbonate (3.2 g), water (80 ml) and methanol (80 ml) was stirred for 6 hours under reflux. The reaction mixture was concentrated under reflux to about 1/3 of the initial volume. The concentrate was subjected to extraction with ethyl acetate. The aqueous layer was acidified with conc. HCl. Resulting crystalline precipitate was collected by filtration to obtain (E)-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzylidenepyruvic acid (1.6 g, 44%). Recrystallization from chloroform-methanol gave colorless needles, m.p.197-198° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06147099 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-ef9c69ce1cf84f8b9d84508161defeab |
| Source note | uspto-grants-2000_11 |