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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643960Generated: November 2, 2026

Sodium Bicarbonate → tert-Butyl 3-(4-benzylpiperazin-1-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1643960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantN,N-Bis(2-chloroethyl)benzylamine hydrochlorideHCID 2777881—
Reactant3-Aminopiperidine hydrochloride, N1-BOC protectedHCID 17750334—
SolventEthanolHCID 702—
Producttert-Butyl 3-(4-benzylpiperazin-1-yl)piperidine-1-carboxylateHCID 86642500—

Reaction Steps

4.90 g (21.1 mmol) of benzylbis(2-chloroethyl)amine hydrochloride were dissolved in ethanol (120 ml) and, while stirring, 5.00 g (21.1 mmol) of tert-butyl 3-aminopiperidine-1-carboxylate hydrochloride and 14.2 g (169 mmol) of sodium bicarbonate were added. The resulting reaction solution was heated under reflux for 4 h. The cooled reaction mixture was concentrated in vacuo, 100 ml of water were added, and the aqueous phase was extracted with ethyl acetate (4×60 ml). The combined organic phases were washed with saturated aqueous NaHCO3 solution, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by chromatography on silica gel (mobile phase gradient 0-5% methanol in dichloromethane). Yield: 6.99 g (75%) of yellow solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119676B2
Source datasetuspto-grants-2012_02
ORD IDord-da4c5a17c36e4fcc914bbcd43242ca4a
Source noteuspto-grants-2012_02