Phenylpyruvic acid
Names | |
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IUPAC name
2-Oxo-3-phenylpropanoic acid | |
Other names
Phenylpyruvate; 3-Phenylpyruvic acid; Keto-phenylpyruvate; beta-Phenylpyruvic acid | |
Identifiers | |
156-06-9 | |
ChEBI | CHEBI:30851 |
ChemSpider | 972 |
| |
Jmol-3D images | Image |
PubChem | 997 |
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Properties | |
Molecular formula |
C9H8O3 |
Molar mass | 164.16 g·mol−1 |
Melting point | 155 °C (311 °F; 428 K) (decomposes) |
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
verify (what is: / ?) | |
Infobox references | |
Phenylpyruvic acid is a pyruvic acid derivative.
Synthesis
Phenylpyruvic acid is synthesized from benzyl chloride by double carbonylation (82% yield).[1][2]
See also
References
- ↑ Wolfram, Joachim. "Preparation of α-keto-carboxylic acids from acyl halides". Google Patents US4481368 & US4481369. Ethyl Corporation.
- ↑ Werner Bertleff, Michael Roeper, & Xavier Sava (2007). "Carbonylation". Ullmann's Encyclopedia of Industrial Chemistry: pg.19. doi:10.1002/14356007.a05_217.pub2.