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HRID 2166262作成日:2026年10月27日

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

https://huagongshe.com/reaction/2166262

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物AzobenzeneHCID 2272—
反応物2,2',4,4'-TetrahydroxybenzophenoneHCID 8571—
反応物FluorenoneHCID 10241—
反応物Sodium HydroxideHCID 14798—
反応物Phenol, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-6-(1,1-dimethylethyl)-4-methyl-HCID 89771—
溶媒1-ButanolHCID 263—
溶媒WaterHCID 962—
生成物2-(2-hydroxy-3-t-butyl-5-methylphenyl)-5-chlorobenzotriazole-N-oxideHCID 14149470829.1%

反応条件

温度65 °C

反応手順

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.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04943637
出典データセットuspto-grants-1990_07
ORD IDord-0480d5fda07e400db85359389b6c23c5
出典メモuspto-grants-1990_07