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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10755Erstellt: 24. Oktober 2026

4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotoluene → 1-Hydroxy-6-(trifluoromethyl)benzotriazole

https://huagongshe.com/de/reaction/10755

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotolueneHCID 8462—
EduktHydrazine hydrate (1:1)HCID 24654—
LösungsmittelEthanolHCID 702—
Produkt1-Hydroxy-6-(trifluoromethyl)benzotriazoleHCID 68819489,5%

Reaktionsschritte

The title compound is prepared according to the procedure described by K. Takeda [J. Org. Chem., 50, 273, (1985)]. A mixture of 4-chloro-3-nitro-α,α,α-trifluorotoluene (50.0 g, 0.22 moles) and hydrazine hydrate (33.0, 0.33 moles) in absolute ethanol (75 ml) is refluxed for 24 h. After removal of the solvent under reduced pressure, the residue is dissolved in 10% aqueous sodium carbonate solution. The solution is washed with ether to remove the starting material and acidified with concentrated HCl to precipitate the product, which is washed with water and dried to obtain 40.0 g of the title compound. This product is recrystallized from ether.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094872B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-868789ba44d24a379570d31b85128dc2
Quellennotizuspto-grants-2006_08