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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372353Generated: October 25, 2026

1-Benzyloxycarbonyl-3-(1-tert-butoxycarbonylaminoethyl)pyrrolidine → tert-butyl N-[1-(pyrrolidin-3-yl)ethyl]carbamate

https://huagongshe.com/reaction/2372353

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyloxycarbonyl-3-(1-tert-butoxycarbonylaminoethyl)pyrrolidineHCID 15228050—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-butyl N-[1-(pyrrolidin-3-yl)ethyl]carbamateHCID 1409901599.1%

Reaction Steps

640 mg of 1-benzyloxycarbonyl-3-(1-tert-butoxycarbonylaminoethyl)pyrrolidine isomer (P-2A) and 300 mg of 5% Pd-C (50% wet) were added to 20 ml of ethanol and catalytic reduction was carried out at room temperature under 3 atm. for 3 h. Then, the catalyst was filtered off and ethanol was distilled off to obtain 390 mg of the desired compound (P-3A) in the form of a colorless, viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05098912
Source datasetuspto-grants-1992_03
ORD IDord-7ed34303c8d34cd69dd4f36f26ccb88e
Source noteuspto-grants-1992_03