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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309396Generated: October 31, 2026

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

https://huagongshe.com/reaction/2309396

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 5.5 N 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 numberUS04695577
Source datasetuspto-grants-1987_09
ORD IDord-24ca289aaea94d0896f57242a1b96e73
Source noteuspto-grants-1987_09