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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273900생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/273900

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참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물2-Hydroxy-4-methoxybenzophenoneHCID 4632—
반응물Sodium MethoxideHCID 10942334—
반응물2-(2-Hydroxy-3-diethylaminomethyl-5-methylphenyl)-2H-benzotriazoleHCID 15919022—
용매MethanolHCID 887—
생성물2-(Benzotriazol-2-yl)-4-methyl-6-(2-hydroxy-3-benzoyl-6-methoxybenzyl)phenolHCID 1991726568.7%

반응 조건

온도130 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05387691
출처 데이터셋uspto-grants-1995_02
ORD IDord-16b52211b7e6495ebc7ee76747d44aa2
출처 메모uspto-grants-1995_02