HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763182Generated: October 31, 2026
Hydroquinone → 2-(2-hydroxy-5-methylphenyl)benztriazole N-oxide
https://huagongshe.com/reaction/1763182
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Azobenzene | HCID 2272 | — |
| Reactant | 4-Methyl-2-[2-(2-nitrophenyl)diazenyl]phenol | HCID 74029 | — |
| Reactant | 2-Nitro-2'-hydroxy-3',5'-bis(tert-amyl)azobenzene | HCID 104111 | — |
| Reactant | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(2-hydroxy-5-methylphenyl)benztriazole N-oxide | HCID 13214646 | 90% |
Reaction Steps
Water 70 ml, 97% sodium hydroxide, 5.2 g, 2-nitro-2'-hydroxy-5'-methylazobenzene 12.9 g and toluene 10 ml were mixed and heated to 60° C. After stirring, hydroquinone 0.6 g was added and glucose 5.0 g was added to the mixture over one hour at 40° to 45° C. The mixture was further stirred for two hours, and the azobenzene disappeared, thus the reaction of Process (b) being completed. The reaction liquor was neutralized with 62% sulfuric acid 5.8 g, and was cooled to 20° C. to precipitate a crystal. The crystal thus precipitated was separated by filtration and was dried, thus producing 10.8 g of 2-(2'-hydroxy-5'-methylphenyl)benzotriazole-N-oxide having a melting point of 138° to 140° C. at the yield of 90.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04835284 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-a8628672157348ffbc214da3deea841c |
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| Source note | uspto-grants-1989_05 |
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