HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756468Generated: October 26, 2026
Octabenzone → 2-(Benzotriazol-2-yl)-4-methyl-6-(2-hydroxy-3-benzoyl-6-n-octyloxybenzyl)phenol
https://huagongshe.com/reaction/1756468
Participants
| Role | Name | HCID | Charge |
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| Reactant | Octabenzone | HCID 15797 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-(2-Hydroxy-3-diethylaminomethyl-5-methylphenyl)-2H-benzotriazole | HCID 15919022 | — |
| Product | 2-(Benzotriazol-2-yl)-4-methyl-6-(2-hydroxy-3-benzoyl-6-n-octyloxybenzyl)phenol | HCID 19917270 | 33.1% |
Reaction Steps
2-(2-Hydroxy-3-diethylaminomethyl-5-methylphenyl)-2H-benzotriazole (21.0 g, 0.067 mol), 2-hydroxy-4-n-octyloxybenzophenone (22.0 g, 0.067 mol), and p-cumene (80 g) are charged to a reaction flask. The mixture is heated to dissolve, and sodium methoxide (1.0 g, 25% in methanol) is added as catalyst. The solution is heated with agitation under a nitrogen flow at reflux (176°-178° C.) for 24 hours. After cooling to room temperature, the solution is filtered, and the black filtered solid (~1 g) is discarded. The product is then precipitated with methanol. The yellow solid (12.5 g) obtained is vacuum filtered, and identified using thin layer chromatography, with toluene:acetone (1:1 ) as the mobile phase. To remove the yellow color, the solid product is dissolved in hot toluene, and silica gel is introduced. The silica gel is gravity filtered hot. The toluene is removed by vacuum distillation, yielding 8.2 g of the title compound as an off-white solid, m.p. 124°-126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05439955 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-c0064b1e096e476fabe8fcf1bc80fe06 |
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| Source note | uspto-grants-1995_08 |
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