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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071388Generated: November 3, 2026

1-(4-Benzylthiobutanoyl)-L-proline → 4-mercaptobutanoyl-L-proline

https://huagongshe.com/reaction/2071388

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Benzylthiobutanoyl)-L-prolineHCID 70074406—
SolventAmmoniaHCID 222—
SolventWaterHCID 962—
Product4-mercaptobutanoyl-L-prolineHCID 22820303—

Reaction Steps

1-(4-Benzylthiobutanoyl)-L-proline (1.08 g.) is dissolved in a mixture of water (4 ml.) and concentrated ammonia (2.7 ml.). After 1 hour stirring at room temperature, the mixture is diluted with water, filtered, extracted with ethyl acetate, and the aqueous phase was concentrated in vacuo. This ammonium salt of 1-(4-mercaptobutanoyl)-L-proline is purified by ion exchange chromatography on a column of diethyl-aminoethyl-Sephadex(cross linked dextran) with a gradient of ammonium bicarbonate, yield 0.7 g. The ammonium salt is dissolved in water (2ml.) and applied to a column of Dowex 50 sulfonic acid resin (analytical grade) in the hydrogen form, and the free acid is eluted with water. The fractions containing the desired material (sulfhydryl reagent and carboxyl reagent positive) are pooled and freeze dried to obtain 1-(4-mercaptobutanoyl)-L-proline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04046889
Source datasetuspto-grants-1977_09
ORD IDord-16a80f7264324dcd8d298949e8ae976e
Source noteuspto-grants-1977_09