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HRID 66126作成日:2026年10月27日

Phenethyl bromide → N-phenethyl-3-methoxyphenethylamine

https://huagongshe.com/reaction/66126

反応式

関与物質

役割名称HCID仕込み量
反応物Phenethyl bromideHCID 7666—
反応物Ammonium HydroxideHCID 14923—
反応物3-MethoxyphenethylamineHCID 74866—
溶媒WaterHCID 962—
生成物N-phenethyl-3-methoxyphenethylamineHCID 1247799747.1%

反応条件

温度165 °C

反応手順

A mixture of 1.51 g of β-(3-methoxyphenyl)-ethylamine and 1.85 g of β-phenethyl bromide was heated to 70°-80° C. on a bath and then was progressively heated to 165° C. over 10 minutes. The mixture was held at 165° C. for 5 minutes and was then cooled. 50 ml of water and then 4 ml of concentrated ammonium hydroxide were added thereto and the mixture was extracted 3 times with 40 ml of methylene chloride. The combined organic extracts were washed with 100 ml of aqueous sodium chloride solution and was dried over magnesium sulfate and was filtered. The filtrate was evaporated to dryness to obtain 3.4 g of raw product which was chromatographed over silica gel. Elution was with a 9-1 chloroform-ethanol mixture and the homogenous fraction with an Rf = 0.45 was taken to obtain 1.2 g of N-phenethyl-3-methoxyphenethylamine in the form of a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04130658
出典データセットuspto-grants-1978_12
ORD IDord-2e873c5bc63843039c95682a71050375
出典メモuspto-grants-1978_12