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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473093Generated: October 30, 2026

Ethanol → Carbamic acid, N-[1-(4-aminophenyl)-4-piperidinyl]-, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/1473093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 12050748HCID 12050748—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductCarbamic acid, N-[1-(4-aminophenyl)-4-piperidinyl]-, 1,1-dimethylethyl esterHCID 12050749—

Reaction Steps

tert-Butyl (1-(4-nitrophenyl)piperidin-4-yl)carbamate (I74) (1.038 g, 3.230 mmol) was dissolved in dry DMF (15 mL), EtOAc (15 mL) and absolute EtOH (15 mL) under an atmosphere of nitrogen. 10% Pd/C (0.200 g) in EtOAc (5 mL) was added to the solution and the atmosphere was changed to hydrogen gas (balloon). The reaction was sealed with balloon and stirred at room temperature for 18 hours. The catalyst was removed by filtration through celite, which was washed with EtOAc (5×10 mL). The solvent was removed in vacuo to give a pink solid which was purified by silica gel chromatography using a gradient of 0-80% ethyl acetate in petroleum benzine 40-60° C. to give the title compound (I75) (0.730 g, 78%) as a purple-brown solid;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012461B2
Source datasetuspto-grants-2015_04
ORD IDord-3f4549376d6b4ee3b85b72c23e9a4504
Source noteuspto-grants-2015_04