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HRID 37191생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-Methoxyphenyl)piperazineHCID 1346—
반응물Sodium IodideHCID 5238—
반응물Potassium CarbonateHCID 11430—
반응물(2-Bromoethyl)tritylamineHCID 15718287—
용매DimethylformamideHCID 6228—
용매AcetonitrileHCID 6342—
생성물2-[4-(2-Methoxyphenyl)piperazin-1-yl]-N-(triphenylmethyl)ethanamineHCID 1571828870.9%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420130
출처 데이터셋uspto-grants-1995_05
ORD IDord-4daa1fcf7cfe48e6859b359d484a1e7b
출처 메모uspto-grants-1995_05