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HRID 1025904作成日:2026年10月27日

2,5-Dichlorophenol → 4-(2,5-Dichloro-phenoxy)-pyrimidine-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1025904

反応式

関与物質

役割名称HCID仕込み量
反応物2,5-DichlorophenolHCID 66—
反応物Cesium carbonateHCID 10796—
反応物Ethyl 4-chloropyrimidine-5-carboxylateHCID 12684326—
触媒tetrakis(acetonitrile)copper(I) hexafluorophosphateHCID 11068737—
溶媒TolueneHCID 1140—
生成物4-(2,5-Dichloro-phenoxy)-pyrimidine-5-carboxylic acid ethyl esterHCID 67320100—

反応手順

To a solution of 420 mg (2.25 mmol) 4-chloropyrimidine-5-carboxylic acid ethyl ester (commercially available, CAS RN 41103-17-7) and 440 mg (2.7 mmol) 2,5-dichlorophenol (commercially available, CAS RN 583-78-8) in 2.5 mL toluene were added 688 mg (5.17 mmol) cesium carbonate and 168 mg (0.45 mmol) tetrakis(acetonitrile) copper(I) hexafluorophosphate (commercially available, CAS RN 64443-05-6). The reaction was heated to reflux for 2.5 h. The solvent was evaporated and the crude reaction product extracted with ethyl acetate from an aqueous saturated solution of sodium bicarbonate. The organic layer was dried over magnesium sulfate, filtered and evaporated. The resulting product was purified by silica gel chromatography using a MPLC system (silica gel column, CombiFlash Companion, Isco Inc.) eluting with a gradient of n-heptane:ethyl acetate yielding 620 mg (88%) of the desired compound as a light yellow viscous oil. MS (ESI): m/z=313.1 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08729091B2
出典データセットuspto-grants-2014_05
ORD IDord-58ab7c6baf114b1ba85ddb0c2160b786
出典メモuspto-grants-2014_05