HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379285Generated: October 30, 2026
Pyridine → (2S,4S)-4-mercapto-2-acetylaminooxymethyl-1-p-nitrobenzyloxycarbonylpyrrolidine
https://huagongshe.com/reaction/2379285
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | HCID 15814452 | HCID 15814452 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2S,4S)-4-mercapto-2-acetylaminooxymethyl-1-p-nitrobenzyloxycarbonylpyrrolidine | HCID 15814453 | 73% |
Reaction Steps
To a solution of (2S,4S)-4-tritylthio-2-acetylaminooxymethyl-l-p-nitrobenzyloxycarbonylpyrrolidine (7a:452 mg) in methanol (9 ml) under ice cooling are dropwise added pyridine (149 μl) and then a solution of silver nitrate (289 mg) in a mixture of water (1.5 ml) and methanol (15 ml), and the mixture is stirred for 25 minutes. Separating silver salt is collected by filtration, washed with methanol, ether, and petroleum ether, and dried. To a suspension of this crude silver salt in a mixture of dichloromethane (3.5 ml) and methanol (3.5 ml) is introduced hydrogen sulfide gas for 5 minutes. The resulting silver sulfide is filtered off and washed with a mixture of methanol and dichloromethane. The filtrate is concentrated in vacuo. The residue is purified by silica gel chromatography to give (2S,4S)-4-mercapto-2-acetylaminooxymethyl-1-p-nitrobenzyloxycarbonylpyrrolidine (8a:198 mg) as a pale yellow foam. Yield: 73%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05360798 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-0dc730030faa43bea6cd855f829a9234 |
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| Source note | uspto-grants-1994_11 |
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