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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2166262생성일: 2026년 10월 26일

Sulfuric Acid → 2-(2-hydroxy-3-t-butyl-5-methylphenyl)-5-chlorobenzotriazole-N-oxide

https://huagongshe.com/reaction/2166262

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물AzobenzeneHCID 2272—
반응물2,2',4,4'-TetrahydroxybenzophenoneHCID 8571—
반응물FluorenoneHCID 10241—
반응물Sodium HydroxideHCID 14798—
반응물Phenol, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-6-(1,1-dimethylethyl)-4-methyl-HCID 89771—
용매1-ButanolHCID 263—
용매WaterHCID 962—
생성물2-(2-hydroxy-3-t-butyl-5-methylphenyl)-5-chlorobenzotriazole-N-oxideHCID 14149470829.1%

반응 조건

온도65 °C

반응 단계

2-nitro-4-chloro-2'-hydroxy-3'-t-butyl-5'-methylazobenzene 23.2 g was added to a mixture of n-butanol 60 g, water 10.6 g and 97% sodium hydroxide 6.9 g, and the resultant mixture was stirred while raising temperature to 65° C. Thereafter, the mixture was cooled to 50° C., and 9-fluorenone 1.5 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 five hours to effect reaction, thus almost all of the azobenzene having disappeared to finish the reaction of Process (b). Thereafter, water 50 ml was added to the reaction mixture, and the mixture was neutralized to pH 8~9 with 62% sulfuric acid 10 g. The neutralized liquor was cooled to 20° C. to precipitate a crystal. The crystal thus precipitated was separated by filtration, thus producing the wet product 22.9 g of 2-(2-hydroxy-3-t-butyl-5-methylphenyl)-5-chlorobenzotriazole-N-oxide (dry product: 20.6 g, yield: 93.0%, melting point: 160°~163° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04943637
출처 데이터셋uspto-grants-1990_07
ORD IDord-0480d5fda07e400db85359389b6c23c5
출처 메모uspto-grants-1990_07