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HRID 52242作成日:2026年10月26日

3-Chloro-p-toluonitrile → 3-(2-chloro-6-fluorophenyl)-5-(3-chloro-4-methylphenyl) 1-methyl-1H-1,2,4-triazole

https://huagongshe.com/reaction/52242

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-p-toluonitrileHCID 88894—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物N-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chlorideHCID 54347086—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物3-(2-chloro-6-fluorophenyl)-5-(3-chloro-4-methylphenyl) 1-methyl-1H-1,2,4-triazoleHCID 2146364755.1%

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 (7.50 g), 3-chloro-4-methylbenzonitrile (3.33 g), anhydrous aluminum chloride (3.00 g) and o-dichlorobenzene (20 ml) is stirred at an oil bath temperature of 140° C. for 1 hour. After cooling, it is washed with saline. Then, it is 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 3.70 g of desired compound.

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-d09da8cf964749938e77b8540c98d8c7
出典メモuspto-grants-1997_04