Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030318Generated: October 26, 2026

Toluene → 2,4-Di-tert-butyl-6-(5-chloro-2H-benzotriazol-2-yl)phenol

https://huagongshe.com/reaction/1030318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2-(2-hydroxy-3,5-di-t-butylphenyl)-5-chlorobenzotriazole-N-oxideHCID 14149471—
Reactant1,5-Diazabicyclo[5.4.0]undeceneHCID 22672070—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
Solvent(+-)-2-ButanolHCID 6568—
Product2,4-Di-tert-butyl-6-(5-chloro-2H-benzotriazol-2-yl)phenolHCID 7747078.8%

Reaction Steps

37.4 g (0.1 mol) of 2-(2'-hydroxy-3',5'-di-t-butylphenyl)-5-chlorobenzotriazole-N-oxide, 0.25 g of Raney nickel catalyst, 150 ml of toluene, 100 ml of 2-butanol and 0.5 g of 1,5-diazabicyclo[5.4.0]undecene were charged into a 500-ml stainless autoclave equipped with an agitator. After the air in the autoclave had been replaced by nitrogen, hydrogen was charged to a pressure of 8 kg/cm2. The temperature of the resultant mixture was increased to 60° C. under agitation, and reaction was been effected while agitation being continued until no hydrogen gas was absorbed by the mixture. After the reaction had been completed, after treatment was performed in the same way as that employed in Example 9 to obtain 28.2 g of 2-(2'-hydroxy-3',5'-di-t-butylphenyl)-5-chlorobenzotriazole as a target substance (yield, 79%; melting point, 153° to 155° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05104992
Source datasetuspto-grants-1992_04
ORD IDord-0027f4a0cd2f44948f6ee117a6e69b2f
Source noteuspto-grants-1992_04