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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273901Generated: October 26, 2026

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

https://huagongshe.com/reaction/273901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOctabenzoneHCID 15797—
ReactantSodiumHCID 5360545—
ReactantSodium MethoxideHCID 10942334—
Reactant2-(2-Hydroxy-3-diethylaminomethyl-5-tert-octylphenyl)-2H-benzotriazoleHCID 15219414—
SolventMethanolHCID 887—
Product2(Benzotriazol2yl)4tert-octyl-6-(2hydroxy-3-benzoyl-6-n-octyloxybenzyl)phenolHCID 1991726762%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387691
Source datasetuspto-grants-1995_02
ORD IDord-52a9089f190f47d9a63727d38ed86d8e
Source noteuspto-grants-1995_02