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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273900Erstellt: 26. Oktober 2026

Toluene → 2-(Benzotriazol-2-yl)-4-methyl-6-(2-hydroxy-3-benzoyl-6-methoxybenzyl)phenol

https://huagongshe.com/reaction/273900

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
Edukt2-Hydroxy-4-methoxybenzophenoneHCID 4632—
EduktSodium MethoxideHCID 10942334—
Edukt2-(2-Hydroxy-3-diethylaminomethyl-5-methylphenyl)-2H-benzotriazoleHCID 15919022—
LösungsmittelMethanolHCID 887—
Produkt2-(Benzotriazol-2-yl)-4-methyl-6-(2-hydroxy-3-benzoyl-6-methoxybenzyl)phenolHCID 1991726568,7%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

2-(2-Hydroxy-3-diethylaminomethyl-5-methylphenyl)-2H-benzotriazole (20.0 g, 0.064 tool), 2-hydroxy-4-methoxybenzophenone (14.7 g, 0,064 mol), and sodium methoxide (1.0 g, 25% in methanol) are charged to a reaction flask. The mixture is heated to 130° C. and held at this temperature for 20 hours with agitation under a nitrogen flow. At that time, the product is identified using thin layer chromatography, with toluene as the mobile phase. To the brown-yellow solid is added hot methanol. The yellow solids are vacuum filtered and triturated twice using methanol, yielding 20.6 g product. To remove the yellow color, the solids are dissolved in hot toluene, and silica gel is introduced. The silica gel is gravity filtered hot. The toluene is removed by vacuum distillation, yielding 12.1 g of the title compound as a pale yellow solid, m.p. 206°-209° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05387691
Quelldatensatzuspto-grants-1995_02
ORD IDord-16b52211b7e6495ebc7ee76747d44aa2
Quellennotizuspto-grants-1995_02