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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308704Generated: November 2, 2026

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

https://huagongshe.com/reaction/2308704

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 from Example 2, 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 reevaporated twice more in the rotary evaporator, the clear oily residue was dissolved in ethyl ether, washed twice with 5% potassium bisulphate 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 numberUS04690938
Source datasetuspto-grants-1987_09
ORD IDord-1c8c119f6a1d45bcb04555f94fe1b8af
Source noteuspto-grants-1987_09