Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260001Generated: November 2, 2026

Pyridine → (2S,4S)-4-mercapto-2-acetylaminooxymethyl-1-p-nitrobenzyloxycarbonylpyrrolidine

https://huagongshe.com/reaction/260001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 15814452HCID 15814452—
CatalystSilver NitrateHCID 24470—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(2S,4S)-4-mercapto-2-acetylaminooxymethyl-1-p-nitrobenzyloxycarbonylpyrrolidineHCID 1581445373%

Reaction Steps

To a solution of (2S,4S)-4-tritylthio-2-acetylaminooxymethyl-1-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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523415
Source datasetuspto-grants-1996_06
ORD IDord-d5f417db1e9949fd85e9357460cb768d
Source noteuspto-grants-1996_06