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HRID 323937作成日:2026年10月23日

Phenol → 3-(4-chlorophenoxy)-N-[3-(imidazol-1-yl)propyl]propionamide

https://huagongshe.com/ja/reaction/323937

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物4-ChlorophenolHCID 4684—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物3-(4-Chlorophenoxy)propionic acidHCID 76780—
反応物1H-Imidazole-1-propanamineHCID 78736—
反応物3-Phenoxypropionic acidHCID 81596—
溶媒TetrahydrofuranHCID 8028—
生成物3-(4-chlorophenoxy)-N-[3-(imidazol-1-yl)propyl]propionamideHCID 18349808—

反応手順

A solution of 3-(4-chlorophenoxy)propionic acid (5.0 g, prepared from 4-chlorophenol by the process described in J.A.C.S. 1923, 2708 for the conversion of phenol into 3-phenoxypropionic acid) in THF (90 ml) was treated with 1,1′-carbonyldiimidazole (4.05 g) at room temperature with stirring. The mixture was stirred at ambient temperature for two hours. 1-(3-Aminopropyl)imidazole (3.12 g) was added and the mixture was stirred at ambient temperature for 18 hours. The solvent was distilled off and the residue was dissolved in dichloromethane, washed with water, dried and then evaporated to give a solid which was recrystallised from ethyl acetate to give 3-(4-chlorophenoxy)-N-[3-(imidazol-1-yl)propyl]propionamide, m.p. 114-115.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06215001B1
出典データセットuspto-grants-2001_04
ORD IDord-d5a1bd3f13494243a5b3d6a235758ca7
出典メモuspto-grants-2001_04