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HRID 26005作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物OctylamineHCID 8143—
反応物Benzene, 1-(3-chloropropoxy)-4-(methylthio)-HCID 12928626—
溶媒EthanolHCID 702—
生成物N-[3-[4-(methylthio)phenoxy]propyl]octylamineHCID 2132617622%

反応手順

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.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04147805
出典データセットuspto-grants-1979_04
ORD IDord-97493774cbfa4cd8a6eab4fe091d5a9d
出典メモuspto-grants-1979_04