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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928542Generated: October 27, 2026

Sodium Iodide → 4-[2-(3,4-Dimethoxy-phenyl)-ethyl]-piperazine-1-carboxylic acid t-butyl ester

https://huagongshe.com/reaction/1928542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant4-(2-Chloroethyl)-1,2-dimethoxybenzeneHCID 3015359—
SolventDimethylformamideHCID 6228—
Product4-[2-(3,4-Dimethoxy-phenyl)-ethyl]-piperazine-1-carboxylic acid t-butyl esterHCID 6699578576.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A reaction mixture of 4-(2-chloroethyl)-1,2-dimethoxybenzene (3.6 g, 17.9 mmol), piperazine-1-carboxylic acid t-butyl ester (4.0 g, 21.5 mmol), K2CO3 (4.97 g, 36 mmol), and NaI (2.7 g, 18 mmol) in DMF (20 mL) was stirred at 80° C. for 3 h, cooled to room temperature, and partitioned between water and ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by column chromatography to afford 4-[2-(3,4-dimethoxy-phenyl)-ethyl]-piperazine-1-carboxylic acid t-butyl ester (4.8 g, 76%) which was dissolved in 4 N HCl in dioxane. This solution was stirred at room temperature for 4 h, concentrated, and dried in a high vacuum oven to give the title compound quantitatively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183374B2
Source datasetuspto-grants-2012_05
ORD IDord-3373b35d914e43e080b0311186816471
Source noteuspto-grants-2012_05