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HRID 1249864作成日:2026年10月25日

2-Chloro-1-iodo-4-nitrobenzene → 2-Chloro-4-nitrobenzotrifluoride

https://huagongshe.com/reaction/1249864

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloro-1-iodo-4-nitrobenzeneHCID 96640—
反応物Potassium FluorideHCID 522689—
反応物(Trifluoromethyl)trimethylsilaneHCID 552549—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物2-Chloro-4-nitrobenzotrifluorideHCID 2778985—

反応手順

A solution of 3-chloro-4-iodo-nitrobenzene (2.26 g), trimethyl(trifluoromethyl)silane (5.68 g), copper(I) iodide (2.28 g), and potassium fluoride (0.56 g) in N,N-dimethylformamide (8 mL) is heated in a sealed tube to 80° C. for 40 hours. The solution is then cooled, diluted with diethyl ether, filtered through diatomaceous earth, and the filtrate is washed successively with water, saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate. The solvent is removed under reduced pressure and the residue is chromatographed over silica gel (1% diethyl ether in hexanes followed by 10% ethyl acetate in hexanes is used as the eluant) to provided the desired product as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06335350B1
出典データセットuspto-grants-2002_01
ORD IDord-7c94974826494364887ed4377befed7f
出典メモuspto-grants-2002_01