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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491218Generated: October 25, 2026

Sodium Bicarbonate → tert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/491218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
Reactant4-(4-Nitrophenyl)piperidineHCID 15925817—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylateHCID 2194008583.2%

Reaction Steps

To a solution of 4-(4-nitrophenyl)piperidine (412 mg, 2 mmol) in CH2Cl2 (100 mL) was added di-tert-butyl carbonate (480 mg, 2.2 mmol) and N,N-dimethylpyridin-4-amine (50 mg, 0.4 mmol). The mixture was stirred for 20 h at room temperature. The mixture was added saturated NaHCO3 (100 mL). The organic layer was separated and aqueous was extracted with CH2Cl2 (50 mL×2). The combined organic solution was dried and concentrated in vacuo. The residue was dissolved in MeOH and bubbled with Ar for 2 min. before adding 10% Pd—C. The hydrogenation was finished in 4 h. The catalyst was removed by filtration and solvent was removed in vacuo to afford title compound (460 mg, 83%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528143B2
Source datasetuspto-grants-2009_05
ORD IDord-85d34c0e64314517801fff44d77b368f
Source noteuspto-grants-2009_05