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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1166345Erstellt: 26. Oktober 2026

p-Tolunitrile → HCID 178425632, Verbindung

https://huagongshe.com/reaction/1166345

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-TolunitrileHCID 7724—
Edukt4-(Methylsulfonyl)anilineHCID 79617—
EduktTrimethylaluminumHCID 16682925—
LösungsmittelTolueneHCID 1140—
LösungsmittelChloroformHCID 6212—
ProduktHCID 178425632HCID 178425632—

Reaktionsschritte

To a suspension of 4-(methylsulfonyl)aniline (3.57 g, 20.9 mmol) in toluene (150 mL), trimethylaluminum (15.6 ml, 2M solution in toluene, 31.4 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 2.5 hours. A solution of 4-methylbenzonitrile (5 ml, 41.8 mmol) in toluene (100 mL) was added over 10 minutes and the reaction mixture heated to 80-85° 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 are concentrated in vacuo and the resulting yellowish solid was stirred with a mixture of hexane/ether (2/1, 600 mL). The intermediate was filtered and washed with more of hexane/ether (2/1). The pale yellow solid 4-methyl-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (5.3 g, 88%) was used in the next reaction without further purification: mp (DSC) 213° C. Anal. Calc'd for C15H16N2SO2: C, 62.48; H, 5.59; N, 9.71. Found: C, 62.00, H, 5.52; N, 9.60.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06613789B2
Quelldatensatzuspto-grants-2003_09
ORD IDord-ce4b3b50e4fd4060b8085455a8e6f07b
Quellennotizuspto-grants-2003_09