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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632375Generated: November 3, 2026

Phenylpyruvic acid → HCID 54264201, compound

https://huagongshe.com/reaction/1632375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylpyruvic acidHCID 997—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 13132286HCID 13132286—
SolventMethanolHCID 887—
ProductHCID 54264201HCID 5426420119.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04474692
Source datasetuspto-grants-1984_10
ORD IDord-f24fdab0526c403eb96b14bca09dc7c8
Source noteuspto-grants-1984_10