HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166260Generated: November 2, 2026
Azobenzene → 2-(2H-Benzotriazol-2-yl)-4,6-bis(tert-pentyl)phenol N-oxide
https://huagongshe.com/reaction/2166260
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobenzene | HCID 2272 | — |
| Reactant | Fluorenone | HCID 10241 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Nitro-2'-hydroxy-3',5'-bis(tert-amyl)azobenzene | HCID 104111 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2H-Benzotriazol-2-yl)-4,6-bis(tert-pentyl)phenol N-oxide | HCID 11143110 | — |
Reaction Steps
2-nitro-2'-hydroxy-3',5'-di-t-amylazobenzene 25.5 g was added to a mixture of n-butanol 80 g, water 14 g and 97% sodium hydroxide 8.2 g, and the resultant mixture was stirred while raising temperature to 65° C. Thereafter, the mixture was cooled to 50° C., and 9-fluorenone 2.0 g was added to the mixture. The reaction mixture was then heated to 90° C. in one hour, and the mixture was stirred at 90°~96° C. for four hours to effect reaction, thus almost all of the azobenzene having disappeared to produce 2-(2-hydroxy-3,5-di-t-amylphenyl)benzotriazole-N-oxide. Thus, the reaction of Process (b) was finished.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04943637 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-476de73c9644423da54a11e78a43ff52 |
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| Source note | uspto-grants-1990_07 |
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