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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972057Generated: October 30, 2026

Carbonic acid, bis(1,1-dimethylethyl) ester → Tert-butyl (1-benzyl-4-hydroxy-4-piperidinyl)methylcarbamate

https://huagongshe.com/reaction/1972057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
Reactant4-(Aminomethyl)-1-benzylpiperidin-4-olHCID 10421026—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductTert-butyl (1-benzyl-4-hydroxy-4-piperidinyl)methylcarbamateHCID 1175902936.6%

Reaction Steps

To a solution of 4-aminomethyl-1-benzyl-piperidin-4-ol (264 mmol, 58 g) in DCM (200 mL) and saturated NaHCO3 (200 mL) was added di-tert-butylcarbonate (396 mmol, 86.4 g). The reaction mixture was stirred for 12 hours. The layers were separated and the organic layer was washed with brine (50 mL) and evaporated. The product was purified on 1 L of SiO2 using a mixtures of ethyl acetate and DCM to give (1-benzyl-4-hydroxy-piperidin-4-ylmethyl)-carbamic acid tert-butyl ester (31 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431575B2
Source datasetuspto-grants-2013_04
ORD IDord-fb0ae1fb15564c21ad1059ec25ac1ec6
Source noteuspto-grants-2013_04