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HRID 52206作成日:2026年10月24日

1,2-Dichlorobenzene → 3-(2-chloro-6-fluorophenyl)-5-(2-chloro-4-nitrophenyl) 1-methyl-1H-1,2,4-triazole

https://huagongshe.com/ja/reaction/52206

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichlorobenzeneHCID 7239—
反応物2-Chloro-4-nitrobenzonitrileHCID 141401—
反応物N-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chlorideHCID 54347086—
触媒Iron chloride (FeCl3)HCID 24380—
溶媒ChloroformHCID 6212—
生成物3-(2-chloro-6-fluorophenyl)-5-(2-chloro-4-nitrophenyl) 1-methyl-1H-1,2,4-triazoleHCID 21463604118.3%

反応条件

温度140 °C

反応手順

A mixture of N-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chloride (1.90 g), 2-chloro-4-nitrobenzonitrile (1.80 g), anhydrous iron (III) chloride (1.60 g) and o-dichlorobenzene (5 ml) is stirred at an oil bath temperature of 140° C. for 1 hour. After cooling, the reaction mixture is dissolved in chloroform (100 ml), washed with dilute hydrochloric acid, dilute aqueous solution of sodium hydroxide and saline in this order, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The concentrate is purified by silica gel column chromatography using mixed solvent of hexane-ethyl acetate as eluent to give 2.20 g of desired compound (melting point: 144.0°-148.0° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616594
出典データセットuspto-grants-1997_04
ORD IDord-d9ee018728f746e7a5dd5c3746938ef1
出典メモuspto-grants-1997_04