돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 330394생성일: 2026년 10월 25일

Triethylamine → N-[2-(Phenylsulfonyl)ethyl]-1-homopiperidineethanamine maleate

https://huagongshe.com/reaction/330394

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물((2-Chloroethyl)sulphonyl)benzeneHCID 13646—
반응물Hexahydro-1H-azepine-1-ethanamineHCID 40002—
반응물Maleic AcidHCID 444266—
용매MethanolHCID 887—
용매AcetonitrileHCID 6342—
생성물N-[2-(Phenylsulfonyl)ethyl]-1-homopiperidineethanamine maleateHCID 7036055760.7%

반응 단계

A mixture of 20.06 g (0.098 mole) of [(2-chloroethyl)sulfonyl]benzene 15.44 g (0.109 mole) of N-(2-aminoethyl)homopiperidine, and 15.0 g (0.149 mole) of triethylamine in 800 ml of acetonitrile was stirred at room temperature for 18 hr. The solvent was removed in vacuo, and the residue was partitioned between methylene chloride and water. The methylene chloride solution was dried over magnesuim sulfate, and the solvent waas removed in vacuo to give an oil. This was dissolved in methanol, and the solution was treated with a solution of 2 equivalents of maleic acid (25.52 g, 0.22 mole) in methanol. A white solid precipitated at room temperature to give 32.3 g (60.7%) of title compound as a white solid; mp 144°-146° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04895840
출처 데이터셋uspto-grants-1990_01
ORD IDord-79450b90b97243f09b921d594904fb8c
출처 메모uspto-grants-1990_01