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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1352925Erstellt: 26. Oktober 2026

Dichloromethane → 4-methylsulfonyl-N-[4-chlorophenyl]benzenecarboximidamide

https://huagongshe.com/reaction/1352925

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt4-FluoroanilineHCID 9731—
Edukt4-(Methylsulfonyl)benzonitrileHCID 519981—
EduktTrimethylaluminumHCID 16682925—
LösungsmittelTolueneHCID 1140—
LösungsmittelChloroformHCID 6212—
Produkt4-methylsulfonyl-N-[4-chlorophenyl]benzenecarboximidamideHCID 17850476335%

Reaktionsschritte

To a suspension of 4-fluoroaniline (4 mL, 40 mmol) in toluene (120 mL), trimethylaluminum (2M solution in toluene, 21 mL, 42 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 3 hours. A solution of 4-(methylsulfonyl)benzonitrile (7.65 g, 40 mmol) in methylene chloride (100 mL) was added over 10 minutes and the reaction mixture was heated to 70–75° C. After 48 hours, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the residue was washed with a mixture of methylene chloride/methanol. The combined filtrates were concentrated in vacuo and the resulting crude intermediate (7.7 g) was purified by chromatography [silica gel, hexane/ethyl acetate, 25/75] to give 4-methylsulfonyl-N-[4-chlorophenyl]benzenecarboximidamide (4.1 g, 35%) as a white solid: mp (DSC) 182° C. Anal. Calc'd. for C14H13N2SO2F: C, 57.52; H, 4.48; N, 9.58; S, 10.97. Found: C, 57.37; H, 4.69; N, 9.21; S, 10.69.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07220770B2
Quelldatensatzuspto-grants-2007_05
ORD IDord-eae5f61ba0f4459cbf7744e93af447e0
Quellennotizuspto-grants-2007_05