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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166254Generated: November 2, 2026

Sulfuric Acid → 2-(2H-Benzotriazol-2-yl)-4,6-bis(tert-pentyl)phenol N-oxide

https://huagongshe.com/reaction/2166254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAzobenzeneHCID 2272—
ReactantFluorenoneHCID 10241—
ReactantSodium HydroxideHCID 14798—
Reactant2-Nitro-2'-hydroxy-3',5'-bis(tert-amyl)azobenzeneHCID 104111—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
Product2-(2H-Benzotriazol-2-yl)-4,6-bis(tert-pentyl)phenol N-oxideHCID 11143110568.8%

Reaction Conditions

Temperature65 °C

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 mixure 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. Thereafter, water 50 ml was added to the reaction liquor, and the reaction liquor was neutralized to pH 8~9 with 62% sulfuric acid 13 g to precipitate a crystal. The crystal thus obtained was filtered to separate the crystal, and the separated crystal was then fully washed with water and further with a small amount of methanol. The washed crystal was then dried, thus producing 23.2 g of 2-(2-hydroxy-3',5'-di-t-amylphenyl)benzotriazole-N-oxide having a melting point of 111° to 113° C. at the yield of 95.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943637
Source datasetuspto-grants-1990_07
ORD IDord-86c5e57c3dee42e9b4e06bc61d6f6619
Source noteuspto-grants-1990_07