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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273901생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/273901

반응식

참여 물질

역할이름HCID투입량
반응물OctabenzoneHCID 15797—
반응물SodiumHCID 5360545—
반응물Sodium MethoxideHCID 10942334—
반응물2-(2-Hydroxy-3-diethylaminomethyl-5-tert-octylphenyl)-2H-benzotriazoleHCID 15219414—
용매MethanolHCID 887—
생성물2(Benzotriazol2yl)4tert-octyl-6-(2hydroxy-3-benzoyl-6-n-octyloxybenzyl)phenolHCID 1991726762%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05387691
출처 데이터셋uspto-grants-1995_02
ORD IDord-52a9089f190f47d9a63727d38ed86d8e
출처 메모uspto-grants-1995_02