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HRID 622402作成日:2026年10月26日

Sodium Hydroxide → 1-(2,4-Dichlorophenyl)-1-(2,4-dichlorophenoxyethoxy)-2-(1,2,4-triazol-1-yl)-1-ethanol

https://huagongshe.com/reaction/622402

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物1-(2-Bromoethoxy)-2,4-dichlorobenzeneHCID 138881—
反応物58905-18-3HCID 662857—
触媒Benzododecinium ChlorideHCID 8753—
溶媒TolueneHCID 1140—
生成物1-(2,4-Dichlorophenyl)-1-(2,4-dichlorophenoxyethoxy)-2-(1,2,4-triazol-1-yl)-1-ethanolHCID 5409101635%

反応手順

12.95 g (0.05 mole) of 1-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)-1-ethanol are dissolved in 100 ml of toluene, and 100 ml of 40% strength sodium hydroxide solution and 1 ml of benzyl-dodecyl-dimethylammonium chloride are added. 13.5 g (0.05 mole) of 2,4-dichlorophenoxyethyl bromide are then added dropwise and the mixture is subsequently stirred at room temperature for 48 hours. The organic phase is separated off, washed with three 100 ml portions of saturated sodium chloride solution, dried over sodium sulphate and concentrated. The residue is taken up in 100 ml of diethyl ether, and crystallizes after the mixture has stood for a short time. 7.8 g (35% of theory) of 1-(2,4-dichlorophenyl)-1-(2,4-dichlorophenoxyethoxy)-2-(1,2,4-triazol-1-yl)-1-ethanol of melting point 88°-90° C. are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04771065
出典データセットuspto-grants-1988_09
ORD IDord-d7a727d7bc5a4a128c7380354907e17c
出典メモuspto-grants-1988_09