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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906143Generated: November 1, 2026

L-Phenylalanine → N-(4-Phenylbutanoyl)-L-phenylalanine

https://huagongshe.com/reaction/1906143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-PhenylalanineHCID 6140—
ReactantSodium CarbonateHCID 10340—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductN-(4-Phenylbutanoyl)-L-phenylalanineHCID 1348812672%

Reaction Steps

The above mentioned ester (13 g) was dissolved in chloroform (200 ml). This solution was added dropwise to the solution obtained by dissolving L-phenylalanine (16.5 g) and Na2CO3 (15.9 g) in water (150 ml) while stirring at room temperature. After that, the mixture was stirred for 7 hours and the insoluble matter thus produced was removed by filtration. The filtrate was acidified to pH 1.0 with 6N HCl. The precipitated crystals were filtered, washed with water, and re-crystallized from 90% aqueous methanol to obtain N-(4-phenylbutyroyl)-L-phenylalanine (11.2 g) having melting point: 178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04650785
Source datasetuspto-grants-1987_03
ORD IDord-57912a5b794c49c7b51b90b114bdfb19
Source noteuspto-grants-1987_03