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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobenzeneHCID 2272—
ReactantFluorenoneHCID 10241—
ReactantSodium HydroxideHCID 14798—
Reactant2-Nitro-2'-hydroxy-5'-t-butylazobenzeneHCID 135514582—
SolventWaterHCID 962—
Solvent(+-)-2-ButanolHCID 6568—
Product2-(2-hydroxy-5-t-butylphenyl)benzotriazole-N-oxideHCID 13907172—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943637
Source datasetuspto-grants-1990_07
ORD IDord-a7d8209b94ae4cad8f47f05e00c7f730
Source noteuspto-grants-1990_07