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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1249864Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1249864

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloro-1-iodo-4-nitrobenzeneHCID 96640—
EduktPotassium FluorideHCID 522689—
Edukt(Trifluoromethyl)trimethylsilaneHCID 552549—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Chloro-4-nitrobenzotrifluorideHCID 2778985—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06335350B1
Quelldatensatzuspto-grants-2002_01
ORD IDord-7c94974826494364887ed4377befed7f
Quellennotizuspto-grants-2002_01