戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 326043作成日:2026年10月26日

Quinoline → Ethyl 2-[4-(2-bromoquinolin-4-yloxy)phenoxy]propionate

https://huagongshe.com/reaction/326043

反応式

関与物質

役割名称HCID仕込み量
反応物QuinolineHCID 7047—
反応物2-Bromo-4-nitroquinolineHCID 581266—
反応物Propanoic acid, 2-(4-hydroxyphenoxy)-, ethyl esterHCID 3017597—
生成物Ethyl 2-[4-(2-bromoquinolin-4-yloxy)phenoxy]propionateHCID 20461964—

反応手順

Ethyl 2-[4-(2-bromoquinolin-4-yloxy)phenoxy]propionate (40) was prepared from 2-bromo-4-nitroquinoline (Chem Abstracts 51: 6639) and ethyl 2-(4-hydroxyphenoxy)-propionate following essentially the same procedure as that described in Example 1. The compound was isolated as a colourless oil which solidified slowly on standing. Proton magnetic resonance spectrum (CDCl3 ; δ in ppm): 8.5-7.4 (4H, m, quinoline protons); 7.1 (4H, d of d, phenyl protons); 6.6 (1H, s, C3 quinoline proton); 4.8 (1H, q, CHCH3); 4.3 (2H, q, OCH2CH3); 1.65 (3H, d, CHCH3); 1.3 (3H t, OCH2CH3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04444584
出典データセットuspto-grants-1984_04
ORD IDord-f2a6132572cd470096f96f4457c7b91f
出典メモuspto-grants-1984_04