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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37191Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/37191

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(2-Methoxyphenyl)piperazineHCID 1346—
EduktSodium IodideHCID 5238—
EduktPotassium CarbonateHCID 11430—
Edukt(2-Bromoethyl)tritylamineHCID 15718287—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-[4-(2-Methoxyphenyl)piperazin-1-yl]-N-(triphenylmethyl)ethanamineHCID 1571828870,9%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05420130
Quelldatensatzuspto-grants-1995_05
ORD IDord-4daa1fcf7cfe48e6859b359d484a1e7b
Quellennotizuspto-grants-1995_05