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HRID 2082168생성일: 2026년 10월 27일

Toluene → 2-(2'-Hydroxy-3'5-di-tert-butylphenyl) benzotriazole

https://huagongshe.com/reaction/2082168

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Sodium HydroxideHCID 14798—
반응물2,4-Bis(1,1-dimethylethyl)-6-[2-(2-nitrophenyl)diazenyl]phenolHCID 104110—
반응물HCID 178418361HCID 178418361—
촉매HCID 178418390HCID 178418390—
용매WaterHCID 962—
용매IsopropanolHCID 3776—
생성물2-(2'-Hydroxy-3'5-di-tert-butylphenyl) benzotriazoleHCID 7745573%

반응 단계

35.5 g (0.1 mol) of 2-nitro-2'-hydroxy-3',5'-di-t-butylazobenzene, 0.125 g of 5% palladium carbon, 100 ml of toluene, 100 ml of IPA, 100 ml water and 8.3 g of caustic soda were charged into a 500-ml stainless autoclave equipped with an agitator. After the air in the autoclave had been replaced by hydrogen, the pressure of hydrogen was set to 10 kg/cm2. Reaction was effected in the same way as that employed in Example 1. After the reaction had been completed, the catalyst was filtered off. When part of the filtrate was subjected to quantitative analysis using GC, it was found that the yield of 2-(2'-hydroxy-3',5'-di-t-butylphenyl)benzotriazole is 82%. After the solvent had been distilled off from the filtrate, the residual solid was crystallized by IPA, washed with IPA and then dried to obtain 23.6 g of 2-(2'-hydroxy-3',5'-di-t-butylphenyl)benzotriazole (yield, 73%; melting point, 150° to 152° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05187289
출처 데이터셋uspto-grants-1993_02
ORD IDord-3d47e57f955241b7acc60e70a49c1ad4
출처 메모uspto-grants-1993_02