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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912392Generated: November 2, 2026

3-Benzyloxycarbonylamino-3-(2-hydroxy-1-methylethyl)piperidine-1-carboxylic acid tert-butyl ester → 3-Amino-3-(2-hydroxy-1-methylethyl)piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1912392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Benzyloxycarbonylamino-3-(2-hydroxy-1-methylethyl)piperidine-1-carboxylic acid tert-butyl esterHCID 58293370—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Product3-Amino-3-(2-hydroxy-1-methylethyl)piperidine-1-carboxylic acid tert-butyl esterHCID 58293281109.3%

Reaction Steps

To a solution of an optically-active compound of 3-benzyloxycarbonylamino-3-(2-hydroxy-1-methylethyl)piperidine-1-carboxylic acid tert-butyl ester (374 mg) in methanol (6 ml) was added 10% palladium carbon (38 mg), and the mixture was hydrogenated at room temperature under ordinary pressure for 14 hours. The mixture was filtered through Celite, and the filtrate was concentrated under reduced pressure to give the titled compound (269 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609647B2
Source datasetuspto-grants-2013_12
ORD IDord-42cd5514ec204078b7234417f9beebdf
Source noteuspto-grants-2013_12