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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37191Generated: October 26, 2026

1-(2-Methoxyphenyl)piperazine → 2-[4-(2-Methoxyphenyl)piperazin-1-yl]-N-(triphenylmethyl)ethanamine

https://huagongshe.com/reaction/37191

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Bromoethyl)tritylamineHCID 15718287—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Product2-[4-(2-Methoxyphenyl)piperazin-1-yl]-N-(triphenylmethyl)ethanamineHCID 1571828870.9%

Reaction Steps

10 g (0.273 mol) of 2-bromo-N-(triphenylmethyl)ethanamine, 200 ml of acetonitrile, 5.15 g (0.0273 mol) of 1-(2-methoxyphenyl)piperazine, 5.6 g of anhydrous potassium carbonate, a few grains of sodium iodide and 1 ml of dimethylformamide are introduced into a 500 ml round-bottomed flask equipped with a reflux condenser and placed under nitrogen. The mixture is heated at reflux for 15 h, the solvents are evaporated, water and dichloromethane are added, the organic phase is separated, washed with water, dried over sodium sulphate and the solvent is evaporated under reduced pressure. A viscous oil is obtained which is purified by chromatography on a column of silica gel, the eluent being a mixture of ethyl acetate and dichloromethane. There are isolated 9.24 g of product which is used as is in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420130
Source datasetuspto-grants-1995_05
ORD IDord-4daa1fcf7cfe48e6859b359d484a1e7b
Source noteuspto-grants-1995_05