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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464978Generated: October 29, 2026

1-Benzyl-3-(tert-butoxycarbonylamino)pyrrolidine → tert-butyl N-(pyrrolidin-3-yl)carbamate

https://huagongshe.com/reaction/464978

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-3-(tert-butoxycarbonylamino)pyrrolidineHCID 3575823—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl N-(pyrrolidin-3-yl)carbamateHCID 27572349.9%

Reaction Steps

A mixture of 101.5 g (0.37 mole) of 1,1-dimethylethyl [1-(phenylmethyl)-3-pyrrolidinyl]carbamate, 5.0 g of 20% Palladium on carbon and 1 liter of tetrahydrofuran was shaken in an atmosphere of hydrogen at about 50 psi and room temperature for 24 hours. The catalyst was removed by filtering through Celite, and the filtrate was concentrated in vacuo to give 6.8 g of 1,1-dimethylethyl (3-pyrrolidinyl)carbamate which solidified upon standing and was of sufficient purity to be used as is for the ensuing steps.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04550103
Source datasetuspto-grants-1985_10
ORD IDord-b052d265133b40e5a166cd937e47120d
Source noteuspto-grants-1985_10