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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252834Generated: November 2, 2026

Ammonia → 1-(3-Mercapto-1-oxopropyl)-L-proline

https://huagongshe.com/reaction/1252834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant3-acetylthiopropanoyl-L-proline-t-butyl esterHCID 13208299—
Product1-(3-Mercapto-1-oxopropyl)-L-prolineHCID 99978—

Reaction Steps

The product of Step (a), 3-acetylthiopropanoyl-L-proline-t-butyl ester (0.5 g) was mixed with 4.5 ml of 5.5N methanolic ammonia at room temperature under nitrogen for one hour to remove the acetyl group. The solvent was then removed at 25° C. with a rotary evaporator. After the product was taken up in methanol and re-evaporated twice more in the rotary evaporator, the clear oily residue was dissolved in ethyl ether, washed twice with 5% potassium bisulfate and once with saturated NaCl, dried over MgSO4 and filtered. Residual solvent was removed in vacuo to yield a clear oily product, migrating as a single spot on thin layer chromatography in three separate solvent systems. The t-butyl ester protecting group was removed by reaction with trifluoroacetic acid in anisole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04745124
Source datasetuspto-grants-1988_05
ORD IDord-6de10f9b52974cbe98d26fa083fef85a
Source noteuspto-grants-1988_05