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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26005생성일: 2026년 10월 23일

Potassium Iodide → N-[3-[4-(methylthio)phenoxy]propyl]octylamine

https://huagongshe.com/ko/reaction/26005

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물OctylamineHCID 8143—
반응물Benzene, 1-(3-chloropropoxy)-4-(methylthio)-HCID 12928626—
용매EthanolHCID 702—
생성물N-[3-[4-(methylthio)phenoxy]propyl]octylamineHCID 2132617622%

반응 단계

A solution of 1-chloro-3-[4-(methylthio)phenoxy]propane (5.0 g., 0.023 mole) in 30 ml. of ethanol is treated with n-octylamine (2.84 g., 0.022 mole) and 30 mg. of potassium iodide. After refluxing for a period of 18 hrs., the reaction mixture is concentrated to dryness under reduced pressure, treated with 3N potassium hydroxide solution and ether, and the layers separated. The ether layer is washed with water, concentrated under reduced pressure, and heated on a steam bath at 0.1 mm Hg pressure to remove residual n-octylamine. The residue of N-[3-[4-(methylthio)phenoxy]propyl]octylamine base thus obtained is dissolved in ethanol, treated with excess 6N hydrochloric acid and activated charcoal, filtered and concentrated to dryness under reduced pressure. Crystallization of the residue from isopropyl alcohol-ether affords 1.7 g. (22% yield) of analytically pure N-[3-[4-(methylthio)phenoxy]propyl]octylamine hydrochloride, m.p. 214.5°-215.5° C. (corr.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04147805
출처 데이터셋uspto-grants-1979_04
ORD IDord-97493774cbfa4cd8a6eab4fe091d5a9d
출처 메모uspto-grants-1979_04