HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255575Generated: October 26, 2026
Ammonia → 1-(3-Mercapto-1-oxopropyl)-L-proline
https://huagongshe.com/reaction/255575
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | 3-acetylthiopropanoyl-L-proline-t-butyl ester | HCID 13208299 | — |
| Product | 1-(3-Mercapto-1-oxopropyl)-L-proline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04698356 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-8d3034b384f3476b86f525cab67b7ebc |
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| Source note | uspto-grants-1987_10 |
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