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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Chloro-p-toluonitrile | HCID 88894 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Edukt | N-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chloride | HCID 54347086 | — |
| Lösungsmittel | 1,2-Dichlorobenzene | HCID 7239 | — |
| Produkt | 3-(2-chloro-6-fluorophenyl)-5-(3-chloro-4-methylphenyl) 1-methyl-1H-1,2,4-triazole | HCID 21463647 | 55,1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05616594 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-d09da8cf964749938e77b8540c98d8c7 |
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| Quellennotiz | uspto-grants-1997_04 |
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