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HRID 273900作成日:2026年10月27日

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

https://huagongshe.com/reaction/273900

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物2-Hydroxy-4-methoxybenzophenoneHCID 4632—
反応物Sodium MethoxideHCID 10942334—
反応物2-(2-Hydroxy-3-diethylaminomethyl-5-methylphenyl)-2H-benzotriazoleHCID 15919022—
溶媒MethanolHCID 887—
生成物2-(Benzotriazol-2-yl)-4-methyl-6-(2-hydroxy-3-benzoyl-6-methoxybenzyl)phenolHCID 1991726568.7%

反応条件

温度130 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05387691
出典データセットuspto-grants-1995_02
ORD IDord-16b52211b7e6495ebc7ee76747d44aa2
出典メモuspto-grants-1995_02