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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371412Generated: November 1, 2026

HCID 22842581, compound → HCID 54147113, compound

https://huagongshe.com/reaction/2371412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22842581HCID 22842581—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54147113HCID 54147113—

Reaction Steps

To a solution of (2R,4R)-1-p-nitrobenzyloxycarbonyl-2-(2-methylaminocarbonylethyl)-4-hydroxypyrrolidine (1.52 g) in tetrahydrofuran (15 ml) and ethanol (15 ml), 10 palladium-carbon (228 mg) was added. The mixture was stirred at room temperature for 3.5 hours under an atmospheric pressure of hydrogen. The reaction mixture was filtered to remove the catalyst. The filtrate was concentrated, and the residue was combined with water, washed with dichloromethane and lyophilized to give (2R,4R)-2-(2-methylaminocarbonylethyl)-4-hydroxypyrrolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05093328
Source datasetuspto-grants-1992_03
ORD IDord-aea0a3eb879a4d34a795ccad280a9e80
Source noteuspto-grants-1992_03