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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757762Generated: October 28, 2026

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

https://huagongshe.com/reaction/1757762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN2 (benzyloxycarbonyl)-N1-tert.butyl-4(R)-hydroxy-L-prolinamideHCID 86746270—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN1-tert.butyl-4(R)-hydroxy-L-prolinamideHCID 57132046108.6%

Reaction Steps

0.224 g of N2 -(benzyloxycarbonyl)-N1 -tert.butyl-4(R)-hydroxy-L-prolinamide was dissolved in 20 ml of ethanol and hydrogenated over 50 mg of 10% palladium-on-carbon at room temperatureand under atmospheric pressure for 2 hours. The catalyst was filtered off and the filtrate was evaporated to give 0.13 g of N1 -tert.butyl-4(R)-hydroxy-L-prolinamide which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446161
Source datasetuspto-grants-1995_08
ORD IDord-deaa3f6edbe04b68b7a182eb8db2609c
Source noteuspto-grants-1995_08