HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273900Generated: October 25, 2026
Toluene → 2-(Benzotriazol-2-yl)-4-methyl-6-(2-hydroxy-3-benzoyl-6-methoxybenzyl)phenol
https://huagongshe.com/reaction/273900
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2-Hydroxy-4-methoxybenzophenone | HCID 4632 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-(2-Hydroxy-3-diethylaminomethyl-5-methylphenyl)-2H-benzotriazole | HCID 15919022 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(Benzotriazol-2-yl)-4-methyl-6-(2-hydroxy-3-benzoyl-6-methoxybenzyl)phenol | HCID 19917265 | 68.7% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05387691 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-16b52211b7e6495ebc7ee76747d44aa2 |
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| Source note | uspto-grants-1995_02 |
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