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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 856612Erstellt: 25. Oktober 2026

Water → (4-Amino-2-trifluoromethylphenyl)(4-methylpyridin-2-yl)methanol

https://huagongshe.com/reaction/856612

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium AzideHCID 33557—
Edukt2-(4-Fluoro-2-trifluoromethylbenzoyl)-4-methylpyridineHCID 22938526—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt(4-Amino-2-trifluoromethylphenyl)(4-methylpyridin-2-yl)methanolHCID 2293851080,3%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

2-(4-fluoro-2-trifluoromethylbenzoyl)-4-methylpyridine (4.5 g) and sodium azide (1.3 g) were suspended in dimethylsulfoxide (30 ml), and the mixture was heated with stirring overnight under nitrogen atmosphere at 90° C. The mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and then, the solvent was evaporated. The residue was dissolved in tetrahydrofuran (30 ml), and to the solution was added aluminum lithium hydride (1.2 g) under ice-cooling, and the mixture was stirred for 1 hour under nitrogen atmosphere under ice-cooling. Water (1.2 ml), 15% aqueous solution of sodium hydroxide (1.2 ml) and water (3.6 ml) were added to the mixture, and the mixture was stirred, dried over anhydrous magnesium sulfate, and filtrated. The solvent of the filtrate was distilled off, to give (4-amino-2-trifluoromethylphenyl)(4-methylpyridin-2-yl)methanol (3.6 g) as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07262185B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-6e182b5deb8b49e48f6c951ea182d770
Quellennotizuspto-grants-2007_08