HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086338Generated: November 1, 2026
Hydrochloric Acid → Sodium 2-oxo-3-phenylbutanoate
https://huagongshe.com/reaction/1086338
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenylpyruvic acid | HCID 997 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Sodium 2-oxo-3-phenylbutanoate | HCID 23676252 | 81% |
Reaction Steps
A 1N aqueous solution of sodium hydroxide (20 ml, 20 mmoles) and 40 ml of methanol were added to 1.64 g (10.0 mmoles) of phenylpyruvic acid to form a solution. Then, 2.0 ml of methyl iodide was added, and the mixture was stirred at room temperature for 10 hours. The reaction mixture was acidified with 1N hydrochloric acid, and extracted with 150 ml of ether. The ether layer was dried over magnesium sulfate and concentrated under reduced pressure to give a pale yellowish white solid. To the solid was added 3 ml of a 3N aqueous solution of sodium hydroxide, and the mixture was concentrated under reduced pressure. Ether was added to the resulting semi-solid mixture, and the precipitated sodium 2-oxo-3-phenylbutanoate was isolated as a white solid (1.62 g; yield 81 %) by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05028738 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-f9e10aa7834042ca9059a2dcd6aabd3a |
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| Source note | uspto-grants-1991_07 |
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