HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166264Generated: October 31, 2026
Azobenzene → 2-(2-hydroxy-5-t-butylphenyl)benzotriazole-N-oxide
https://huagongshe.com/reaction/2166264
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobenzene | HCID 2272 | — |
| Reactant | Fluorenone | HCID 10241 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Nitro-2'-hydroxy-5'-t-butylazobenzene | HCID 135514582 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | (+-)-2-Butanol | HCID 6568 | — |
| Product | 2-(2-hydroxy-5-t-butylphenyl)benzotriazole-N-oxide | HCID 13907172 | — |
Reaction Steps
9-fluorenone 2.5 g was added to a mixture of secondary butanol 80 g, water 14 g and 97% sodium hydroxide 22.4 g, and 2-nitro-2'-hydroxy-5'-t-butylazobenzene 19.9 g was added to the resultant mixture for one hour while stirring at 80° C. The mixture was further stirred at 90°~97° C. for 4 hours, thus almost all of the azobenzene having disappeared to produce 2-(2-hydroxy-5-t-butylphenyl)benzotriazole-N-oxide. Thus, the reaction of Process (b) was completed. The resultant reaction liquor was further stirred for 4 hours, thus the N-oxide having disappeared to finish the reaction of Process (c).
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-a7d8209b94ae4cad8f47f05e00c7f730 |
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| Source note | uspto-grants-1990_07 |
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