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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600903Generated: October 30, 2026

3-(R)-[1-[N-(tert-butoxycarbonyl)-N-(ethyl)Amino]Cyclopropyl]-1-[1-(S)-phenylethyl]Pyrrolidine → 3-(R)-[1-[N-(tert-butoxycarbonyl)-N-(ethyl)amino]cyclopropyl]pyrrolidine

https://huagongshe.com/reaction/600903

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(R)-[1-[N-(tert-butoxycarbonyl)-N-(ethyl)Amino]Cyclopropyl]-1-[1-(S)-phenylethyl]PyrrolidineHCID 67271934—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product3-(R)-[1-[N-(tert-butoxycarbonyl)-N-(ethyl)amino]cyclopropyl]pyrrolidineHCID 67270724—

Reaction Conditions

Temperature40 °C

Reaction Steps

3-(R)-[1-[N-(tert-butoxycarbonyl)-N-(ethyl)amino]cyclopropyl]-1-[1-(S)-phenylethyl]pyrrolidine (3.01 g, 8.40 mmol) was dissolved in ethanol (120 ml), and after adding a 10% palladium carbon catalyst (water content: 50%; 3.0 g), it was stirred at 40° C. for 5 hours under a hydrogen atmosphere at atmospheric pressure. After performing filtration through cellite (ethanol washing), the filtrate was concentrated under a reduced pressure. As a result, 2.16 g (quantitative) of the title compound was obtained in the form of a colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902226B2
Source datasetuspto-grants-2011_03
ORD IDord-fe82bc07047d40818c3561c6ab4b6421
Source noteuspto-grants-2011_03