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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466883Generated: October 29, 2026

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

https://huagongshe.com/reaction/466883

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 temperature and 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 numberUS05157041
Source datasetuspto-grants-1992_10
ORD IDord-2c15159b070d4529b06f9670840fafe6
Source noteuspto-grants-1992_10