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HRID 273901作成日:2026年10月26日

Octabenzone → 2(Benzotriazol2yl)4tert-octyl-6-(2hydroxy-3-benzoyl-6-n-octyloxybenzyl)phenol

https://huagongshe.com/reaction/273901

反応式

関与物質

役割名称HCID仕込み量
反応物OctabenzoneHCID 15797—
反応物SodiumHCID 5360545—
反応物Sodium MethoxideHCID 10942334—
反応物2-(2-Hydroxy-3-diethylaminomethyl-5-tert-octylphenyl)-2H-benzotriazoleHCID 15219414—
溶媒MethanolHCID 887—
生成物2(Benzotriazol2yl)4tert-octyl-6-(2hydroxy-3-benzoyl-6-n-octyloxybenzyl)phenolHCID 1991726762%

反応手順

Methanol (50 ml) is placed into a 300 ml three-necked flask equipped with a stirrer, thermometer, condenser, Dean-Stark trap and nitrogen inlet. Sodium (0.3 g, 0.013 tool) is added to the methanol and the mixture stirred at room temperature till all the sodium is dissolved. Then, 2-(2-hydroxy-3-diethylaminomethyl-5-tert-octylphenyl)-2H-benzotriazole (10.2 g, 0.025 mol), 2-hydroxy-4-n-octyloxybenzophenone (8.2 g, 0.025 mol) and another 50 ml of methanol are added to the sodium methoxide solution. The reactants are heated at reflux till half the methanol is collected in the Dean-Stark trap. o-Xylene (50 ml) is added and the temperature is raised to the reflux temperature of o-xylene (143°-145° C.) and heating is continued for 24 hours. The mixture is then cooled and acetic acid is added to neutralize the sodium methoxide catalyst. The o-xylene solvent is then removed by vacuum distillation. The crude product obtained is recrystallized from heptane to afford the title compound in a yield of 10 g (62 % yield) as a white crystalline solid melting at 96°-100° 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-52a9089f190f47d9a63727d38ed86d8e
出典メモuspto-grants-1995_02