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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758842Generated: November 1, 2026

2-Oxo-4-phenylbutyric acid → HCID 13105154, compound

https://huagongshe.com/reaction/1758842

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Oxo-4-phenylbutyric acidHCID 69732—
ReactantL-Alanyl-L-prolineHCID 83525—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventWaterHCID 962—
ProductHCID 13105154HCID 13105154—

Reaction Steps

A mixture of 4-phenyl-2-oxobutyric acid (1.49 g) and L-alanyl-L-proline (0.31 g) in water are adjusted to pH 7.5 with caustic and treated with sodium cyanoborohydride (0.32 g) overnight. The product is absorbed on strong acid ion exchange resin and eluted with 2% pyridine in water to give 0.36 g of crude diastereomeric product, N-(1-carboxy-3-phenylpropyl)-L-alanyl-L-proline. A portion is purified by gel filtration (LH-20) for spectrographic analysis. The nmr spectrum in DMSO shows aromatic hydrogen at 7.20, a broad singlet at 4.30, broad multiplets at 3.0 to 3.9, 2.67 and 1.94, and a doublet at 1.23 and 1.15. The mass spectrum shows a molecular ion at 492 m/e for the ditrimethylsilylated species.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04374829
Source datasetuspto-grants-1983_02
ORD IDord-cc7b93ae6ac14215ad4830a8ad99f9f8
Source noteuspto-grants-1983_02