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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 330393생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/330393

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물((2-Chloroethyl)sulphonyl)benzeneHCID 13646—
반응물N-(2-Aminoethyl)piperidineHCID 33944—
반응물Maleic AcidHCID 444266—
용매MethanolHCID 887—
용매AcetonitrileHCID 6342—
생성물N-[2-(Phenylsulfonyl)ethyl]-1-piperidineethanamine maleateHCID 7036054360.78%

반응 단계

A mixture of 40.94 g (0.20 mole) of [(2-chloroethyl)sulfonyl]benzene, 27.85 g (0.217 mole) of N-(2-aminoethyl)piperidine and 28.0 g (0.277 mole) of triethylamine in 800 ml of acetonitrile was stirred at room temperature overnight. The solvent was removed in vacuo, and the residue was partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride solution was dried over magnesium sulfate, and the solvent was removed in vacuo. The residue was dissolved in methanol, a solution of 2 equivalents of maleic acid in methanol was added, and the product crystallized from the solution at room temperatue to give 64.35 g (60.78%) of title compound as a white crystalline solid, mp 154°-155.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04895840
출처 데이터셋uspto-grants-1990_01
ORD IDord-02a04086823f4a4e8450854c0a958793
출처 메모uspto-grants-1990_01