HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868708Generated: October 27, 2026
Acetaldehyde → 2-(2-hydroxy-5-methylphenyl)benztriazole N-oxide
https://huagongshe.com/reaction/868708
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Fluorenone | HCID 10241 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Methyl-2-[2-(2-nitrophenyl)diazenyl]phenol | HCID 74029 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-hydroxy-5-methylphenyl)benztriazole N-oxide | HCID 13214646 | — |
Reaction Steps
2-nitro-2'-hydroxy-5'-methylazobenzene 12.9 g was added to a mixture of methanol 60 ml, water 30 ml and 97% sodium hydroxide 12.4 g, and the resultant mixture was stirred while raising temperature to 65° C. 9-fluorenone 1.2 g and then 90% acetoaldehyde 3.2 g were added to the mixture for 1 hour. The resultant mixture was then heated to the boiling point (75° C.), and was stirred at the boiling point (75° C.) for 6 hours, thus almost all of the azobenzenes having disappeared to produce 2-(2-hydroxy-5-methylphenyl)benzotriazole-N-oxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04780541 |
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| Source dataset | uspto-grants-1988_10 |
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| ORD ID | ord-d97cab669722445baf11994c637087f9 |
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| Source note | uspto-grants-1988_10 |
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