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HRID 325831作成日:2026年10月26日

Dimethyl Sulfoxide → 2-[5-(2-Cyano-4-fluorophenoxy)-2-methylthiophenoxy]propionamide

https://huagongshe.com/reaction/325831

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物WaterHCID 962—
反応物2-BromopropanamideHCID 101118—
反応物5-(2-Cyano-4-fluorophenoxy) 2-(methylthio)phenolHCID 20462849—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物2-[5-(2-Cyano-4-fluorophenoxy)-2-methylthiophenoxy]propionamideHCID 131713486—

反応手順

5-(2-Cyano-4-fluorophenoxy)-2-(methylthio)phenol (0.05 mole) potassium carbonate (0.2 mole), 2-bromopropionamide (0.08 mole) and dimethylsulfoxide (200 ml) are charged into a 500 ml glass reaction flask equipped with a mechanical stirrer. The reaction mixture is stirred at room temperature for a period of about 8 hours. After this time the mixture is poured into 500 ml of water. The resulting mixture is extracted three times with 100 ml portions of methylene chloride. The extracts are then combined, washed with water and thereafter dried. The dried solution is then stripped of solvent under reduced pressure to leave a residue. The residue is subjected to chromatography using a clay column and hexane/ethyl acetate mixtures as the eluant. The fractions containing the product are combined and stripped of solvent to yield the desired product 2-[5-(2-cyano-4-fluorophenoxy)-2-methylthiophenoxy]propionamide as the residue.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04443248
出典データセットuspto-grants-1984_04
ORD IDord-558b3d313b6544dda8e9439e419a4d5b
出典メモuspto-grants-1984_04