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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39700Generated: October 26, 2026

4-Benzyloxycarbonylamino-4-hydroxymethyl piperidine-1-carboxylic acid tert-butyl ester → tert-Butyl 4-amino-4-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/39700

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyloxycarbonylamino-4-hydroxymethyl piperidine-1-carboxylic acid tert-butyl esterHCID 66741770—
CatalystHCID 178502593HCID 178502593—
SolventEthanolHCID 702—
Producttert-Butyl 4-amino-4-(hydroxymethyl)piperidine-1-carboxylateHCID 22975819—

Reaction Conditions

Temperature40 °C

Reaction Steps

To 10 mL of an ethanol solution containing 0.55 g of tert-butyl 4-(((benzyloxy)carbonyl)amino)-4-(hydroxymethyl)piperidine-1-carboxylate, 0.10 g of 20% palladium hydroxide-carbon was added at room temperature, and the mixture was stirred at 40° C. for 3 hours under a hydrogen atmosphere. The insoluble material filtered off, and the filtration residue thus obtained was washed 3 times with chloroform. The filtrate and the washing solution were combined, and the solvent was removed under reduced pressure to obtain 0.39 g of a dark brown oily substance, tert-butyl 4-amino-4-(hydroxymethyl)piperidine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524738B2
Source datasetuspto-grants-2013_09
ORD IDord-c24a0a827f9e4dfc85ef3b68c16bd8a9
Source noteuspto-grants-2013_09