2,2,2-Trifluoroethanol → HCID 59570318, compound

Participants

Reaction Steps

Into 5 ml of tetrahydrofuran was suspended 0.12 g of sodium hydride (60% oily), and 0.27 g of trifluoroethyl alcohol was added at 10° C. After stirring for 10 minutes, 0.5 g of 3,4,5-trichloropyridine-2-carbonitrile was added at 0° C., the mixture was stirred for 20 hours, and the reaction solution was poured into an aqueous saturated ammonium chloride solution, followed by extraction with tert-butyl=methyl=ether three times. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.6 g of 3,5-dichloro-4-(2,2,2-trifluoroethoxy)pyridine-2-carbonitrile. 3,5-Dichloro-4-(2,2,2-trifluoroethoxy)pyridine-2-carbonitrile

Provenance & Evidence