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HRID 868175Erstellt: 25. Oktober 2026

Triethylamine → 6-Trifluoromethoxy-1-trifluoromethylsulphenylindazole

https://huagongshe.com/reaction/868175

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfenyl chloride, trifluoro-HCID 67900—
Edukt6-(Trifluoromethoxy)-1H-indazoleHCID 13712997—
LösungsmittelTolueneHCID 1140—
Produkt6-Trifluoromethoxy-1-trifluoromethylsulphenylindazoleHCID 13713012—

Reaktionsschritte

20.2 g (0.1 mole) of 6-trifluoromethoxyindazole and 10.1 g (0.1 mole) of triethylamine in 125 ml of toluene are heated to 80° to 85° C., and 13.6 g (0.1 mole) of trifluoromethanesulphenyl chloride are then passed in the course of one hour and the mixture is stirred for a further hour at this temperature. After cooling, the precipitated triethylamine hydrochloride is filtered off with suction and rinsed with toluene. The filtrate, combined with the wash liquor, is washed twice with water. After drying (MgSO4) the volatile constituents are removed by distillation under a water pump vacuum. The oily crude product is purified by distillation under an oil pump vacuum. Boiling point 62°/0.05 mbar. Yield: 16.2 g (46% of theory).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04778511
Quelldatensatzuspto-grants-1988_10
ORD IDord-ffd70e6dcf6542288e1094786099fbe2
Quellennotizuspto-grants-1988_10