戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 12421作成日:2026年10月23日

Dimethylformamide → 2(1H)-Pyridinone,1-(4-methoxyphenyl)-5-(trifluoromethyl)-

https://huagongshe.com/ja/reaction/12421

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物4-IodoanisoleHCID 69676—
反応物2-Hydroxy-5-(trifluoromethyl)pyridineHCID 147443—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒AmmoniaHCID 222—
生成物2(1H)-Pyridinone,1-(4-methoxyphenyl)-5-(trifluoromethyl)-HCID 1198894439.2%

反応条件

温度135 °C

反応手順

A mixture of 5-(trifloromethyl)-2(1H)-pyridone (815.5 mg, 5 mmol), 4-iodoanisole (2.34 g, 10 mmol), CuI (952 mg, 5 mmol), K2CO3 (691 mg, 5 mmol) and DMF (5 ml) was heated at 135° C. overnight. The reaction mixture was diluted with 10% ammonia (15 ml) and extracted with ethyl acetate. The organic extract was washed with saturated sodium chloride, dried over magnesium sulfate and evaporated. Column chromatography purification (30% ethyl acetate-hexane) afforded 526 mg (39.2%) of 1-(4-methoxyphenyl)-5-(trifloromethyl)-2-pyridone. This compound (268.2 mg, 1 mmol) was treated with 1M BBr3 solution in dichloromethane (DCM, 2 ml) in DCM (5 ml) for 2 hours at 0° C. Reaction mixture was diluted with DCM and washed 3 times with water. Organic phase was dried over sodium sulfate and evaporated. The residue was separated by column chromatography (20% ethyl acetate-DCM) to afford the title compound as a off-white solid, 226 mg (89%). The 1H NMR spectra was consistent with the structure of Compound 10.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728013B2
出典データセットuspto-grants-2010_06
ORD IDord-acab1f45784f4d8e9846f2a7af06e5b9
出典メモuspto-grants-2010_06