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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252815Generated: November 3, 2026

N-(3-benzoylthiopropanoyl)-L-alanine → N-(3-Sulfanylpropanoyl)-L-alanine

https://huagongshe.com/reaction/1252815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-benzoylthiopropanoyl)-L-alanineHCID 13036931—
SolventWaterHCID 962—
SolventAmmonium HydroxideHCID 14923—
ProductN-(3-Sulfanylpropanoyl)-L-alanineHCID 1303694070.7%

Reaction Steps

N-(3-benzoylthiopropanoyl)-L-alanine (4.2 g) is dissolved in a mixture of water (7.5 ml) and concentrated ammonium hydroxide (6 ml). After one hour, the mixture is diluted with water, filtered and the filtrate is extracted with ethyl acetate. The aqueous phase is acidified with concentrated hydrochloric acid and extracted with ethyl acetate. The organic phase is washed with water, dried and concentrated to dryness in vacuo. The residue is crystallized from ethyl acetate-hexane to yield 1.87 g of N-(3-mercaptopropanoyl)-L-alanine, m.p. 79°-81°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04745124
Source datasetuspto-grants-1988_05
ORD IDord-9116ed926520467993fe44e21630607f
Source noteuspto-grants-1988_05