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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466889Generated: October 29, 2026

N2 (benzyloxycarbonyl)-4(R)-(tert-butoxyformamido)-N1-tert.butyl-L-prolinamide → 4(R)-(tert-butoxyformamido)-N1-tert.butyl-L-prolinamide

https://huagongshe.com/reaction/466889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN2 (benzyloxycarbonyl)-4(R)-(tert-butoxyformamido)-N1-tert.butyl-L-prolinamideHCID 86746286—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4(R)-(tert-butoxyformamido)-N1-tert.butyl-L-prolinamideHCID 57267270106.6%

Reaction Steps

0.25 g of N2 -(benzyloxycarbonyl)-4(R)-(tert.butoxyformamido)-N1 -tert.butyl-L-prolinamide was dissolved in ethanol and hydrogenated over 0.1 g of 10% palladium-on-carbon at room temperature and under atmospheric pressure for 4 hours. The catalyst was filtered off and the filtrate was evaporated to give 0.17 g of 4(R)-(tert.butoxyformamido)-N1 -tert.butyl-L-prolinamide as a glass which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157041
Source datasetuspto-grants-1992_10
ORD IDord-c6c23a283d6c4a39852bf479189d596c
Source noteuspto-grants-1992_10