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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354071Generated: October 30, 2026

Benzyl 4-((tert-butoxycarbonyl)(methyl)amino)piperidine-1-carboxylate → 4-N-Boc-4-N-Methyl-aminopiperidine

https://huagongshe.com/reaction/2354071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-((tert-butoxycarbonyl)(methyl)amino)piperidine-1-carboxylateHCID 20782499—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-N-Boc-4-N-Methyl-aminopiperidineHCID 2756806—

Reaction Steps

A mixture of 4-(tert-butoxycarbonyl-methyl-amino)-piperidine-1-carboxylic acid benzyl ester (17.5 mmol) and Pd—C (10%, 500 mg) in MeOH (150 mL) hydrogenated at atm. pressure and r.t. for 15 h. The mixture is filtered and evaporated. The residue is dissolved in CH2Cl2 (100 mL) and 1 M aq. NaOH (50 mL) is added. The mixture is stirred for 6 h at r.t., then the phases are separated and the aq. phase is extracted with CH2Cl2 (3×50 mL). The combined organic extracts are dried (Na2SO4), filtered and evaporated to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750161B2
Source datasetuspto-grants-2010_07
ORD IDord-a68a6ca851604ecaaecb05539ba0318f
Source noteuspto-grants-2010_07