HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632375Generated: November 3, 2026
Phenylpyruvic acid → HCID 54264201, compound
https://huagongshe.com/reaction/1632375
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylpyruvic acid | HCID 997 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 13132286 | HCID 13132286 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54264201 | HCID 54264201 | 19.2% |
Reaction Steps
L-Alanyl-N-(indan-2-yl)glycine (1.0 g) and 6.0 g of phenylpyruvic acid are dissolved in 50 ml of 70% aqueous methanol, and the pH is adjusted to 7.0 with aqueous potassium hydroxide. Sodium cyanoborohydride (1.0 g) is added to this solution. After allowing the mixture to stand at room temperature overnight, the solvent is distilled off under reduced pressure, the residue is dissolved in 2 ml of water, made adsorbed on a Dowex 50 (H+) [trade name of ion-exchange resin] column and eluted with 2% pyridine. The solvent is distilled off under reduced pressure, the residue is purified by silica gel column chromatography using acetonitrile-methanol (4:1) as the developer to give 0.3 g of N-(1-carboxy-2-phenylethyl)-L-alanyl-N-(indan-2-yl)glycine as colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04474692 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-f24fdab0526c403eb96b14bca09dc7c8 |
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| Source note | uspto-grants-1984_10 |
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