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HRID 1433344作成日:2026年10月25日

3-Fluoro-4-nitrophenol → 6-Cyano-4-(3-fluoro-4-nitrophenoxy)-7-(2-methoxyethoxy)quinoline

https://huagongshe.com/reaction/1433344

反応式

関与物質

役割名称HCID仕込み量
反応物3-Fluoro-4-nitrophenolHCID 520948—
反応物4-Chloro-6-cyano-7-(2-methoxyethoxy)quinolineHCID 22646522—
溶媒ChlorobenzeneHCID 7964—
生成物6-Cyano-4-(3-fluoro-4-nitrophenoxy)-7-(2-methoxyethoxy)quinolineHCID 2293657362.5%

反応手順

4-Chloro-6-cyano-7-(2-methoxyethoxy)quinoline (1.7 g) and 3-fluoro-4-nitrophenol (2.0 g) were suspended in chlorobenzene (20 ml), and the suspension was heated to reflux for 6 hours. After completion of the reaction, the solvent was distilled off, ethyl acetate was added, and a solid precipitated. The solid was filtered out and washed with ether, washed with 1N sodium hydroxide water and with water, and then dried to obtain 1.55 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07612092B2
出典データセットuspto-grants-2009_11
ORD IDord-a5d23096790d411896c9bf53441d7f88
出典メモuspto-grants-2009_11