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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 52312Erstellt: 24. Oktober 2026

4-(Methylsulfonyl)aniline → HCID 178425633, Verbindung

https://huagongshe.com/de/reaction/52312

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(Methylsulfonyl)anilineHCID 79617—
Edukt3-Chloro-p-toluonitrileHCID 88894—
EduktTrimethylaluminumHCID 16682925—
LösungsmittelTolueneHCID 1140—
LösungsmittelChloroformHCID 6212—
ProduktHCID 178425633HCID 178425633—

Reaktionsschritte

To a suspension of 4-(methylsulfonyl)aniline (2.82 g, 16.5 mmol) in toluene (150 mL), trimethylaluminum (2M solution in toluene, 12.5 mL, 24.7 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 2.5 hours. A solution of 3-chloro-4-methylbenzonitrile (5 g, 33 mmol) in toluene (100 mL) was added over 10 minutes and the reaction mixture was heated to 90°-95° C. After 20 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 (2/1). The combined filtrates were concentrated in vacuo and the resulting yellowish solid was stirred with a mixture of hexane/ether (2/1, 700 mL). The intermediate was filtered and washed with more of hexane/ether (2/1). The pale yellow solid 3-chloro-4-methyl-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (4.7 g, 88%) was used in the next reaction without further purification: mp (DSC) 179° C. Anal. Calc'd. for C15H15N2SO2Cl: C, 55.81, H, 4.68, N, 8.68. Found: C, 55.65, H, 4.63, N, 8.59.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05616601
Quelldatensatzuspto-grants-1997_04
ORD IDord-b3b0a34bbebd4c4f8d05de58db324efd
Quellennotizuspto-grants-1997_04