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HRID 623708Erstellt: 24. Oktober 2026

Pyridine → 2-(2,4-difluorophenyl)-4,5-dimethyl-2H-1,2,3-triazole 1-oxide

https://huagongshe.com/de/reaction/623708

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt2,4-Difluorophenylhydrazine hydrochlorideHCID 2733301—
EduktIsonitrosoacetoneHCID 6399095—
KatalysatorCopper sulfate pentahydrateHCID 24463—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-(2,4-difluorophenyl)-4,5-dimethyl-2H-1,2,3-triazole 1-oxideHCID 90109810—

Reaktionsbedingungen

Temperatur23 °C

Reaktionsschritte

To a stirred solution of anti-pyruvic aldehyde 1-oxime (2.2 g, 22.2 mmol) in diethyl ether (50 mL) was added 2,4-difluorophenylhydrazine hydrochloride (4.0 g, 22.2 mmol) and pyridine (2 mL). The reaction mixture was stirred at 23° C. for 64 h. The solid that formed was removed by filtration and washed with diethyl ether. The filtrate was concentrated under reduced pressure. The crude residue was dissolved in pyridine (100 mL). A solution of copper(II) sulfate pentahydrate (11.1 g, 44.4 mmol) in water (60 mL) was added at once and the resulting mixture was stirred at reflux for 20 h. The mixture was diluted with water and extracted with diethyl ether. The combined organic layers were washed with 1.0 M aqueous hydrochloric acid, dried (MgSO4) and concentrated under reduced pressure to afford the crude product. The crude material was purified by chromatography on silica gel eluting with 0 to 100% ethyl acetate in hexanes to obtain the title compound (1.98 g) as an orange solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09302999B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-8a8bc382c165408fb7cb9611391531c6
Quellennotizuspto-grants-2016_04