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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 52242Erstellt: 23. Oktober 2026

3-Chloro-p-toluonitrile → 3-(2-chloro-6-fluorophenyl)-5-(3-chloro-4-methylphenyl) 1-methyl-1H-1,2,4-triazole

https://huagongshe.com/de/reaction/52242

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Chloro-p-toluonitrileHCID 88894—
EduktAluminum(III) ChlorideHCID 6451240—
EduktN-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chlorideHCID 54347086—
Lösungsmittel1,2-DichlorobenzeneHCID 7239—
Produkt3-(2-chloro-6-fluorophenyl)-5-(3-chloro-4-methylphenyl) 1-methyl-1H-1,2,4-triazoleHCID 2146364755,1%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

A mixture of N-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chloride (7.50 g), 3-chloro-4-methylbenzonitrile (3.33 g), anhydrous aluminum chloride (3.00 g) and o-dichlorobenzene (20 ml) is stirred at an oil bath temperature of 140° C. for 1 hour. After cooling, it is washed with saline. Then, it is dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The concentrate is purified by silica gel column chromatography using mixed solvent of hexane-ethyl acetate as eluent to give 3.70 g of desired compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05616594
Quelldatensatzuspto-grants-1997_04
ORD IDord-d09da8cf964749938e77b8540c98d8c7
Quellennotizuspto-grants-1997_04