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HRID 227553作成日:2026年10月24日

3,5-Bis(trifluoromethyl)phenylacetic acid → 2-[4-{[3,5-Bis(trifluoromethyl)phenyl]acetyl}-2-(3,4-dichlorophenyl)morpholin-2-yl]ethanol

https://huagongshe.com/ja/reaction/227553

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-Bis(trifluoromethyl)phenylacetic acidHCID 123587—
反応物2-[2-(3,4-Dichlorophenyl)morpholin-2-YL]ethanolHCID 15472747—
溶媒AcetonitrileHCID 6342—
生成物2-[4-{[3,5-Bis(trifluoromethyl)phenyl]acetyl}-2-(3,4-dichlorophenyl)morpholin-2-yl]ethanolHCID 1867720558.6%

反応手順

To a solution of 3,5-bis(trifluoromethyl)phenylacetic acid (2.0 g, 7.4 mmol) in acetonitrile (20 ml), N,N′-carbonyldiimidazole (1.3 g, 8.1 mmol) was added at room temperature, then 2-[2-(3,4-dichlorophenyl)morpholin-2-yl]ethanol (2.4 g, 8.8 mmol) was further added, and the resulting mixture was stirred at room temperature for one hour. After completion of the reaction, the reaction mixture was evaporated to dryness. To the obtained residue, methylene chloride (20 ml), water (20 ml) and concentrated hydrochloric acid (2 ml) were added, and the resulting mixture was partitioned. The separated organic layer was washed successively with a 5% aqueous solution of sodium hydroxide (25 ml) and water (20 ml) and evaporated to dryness to afford the title compound [2.3 g, yield: 58.6%] as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560549B2
出典データセットuspto-grants-2009_07
ORD IDord-55f01e0ef7054611848a4ecce95d2639
出典メモuspto-grants-2009_07