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HRID 37443作成日:2026年10月25日

1-Chloro-4-(chloromethyl)benzene → 1-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazine

https://huagongshe.com/reaction/37443

反応式

関与物質

役割名称HCID仕込み量
反応物1-Chloro-4-(chloromethyl)benzeneHCID 7723—
反応物DiisopropylamineHCID 7912—
反応物4-Methoxyphenylhydrazine hydrochlorideHCID 2723904—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒DichloromethaneHCID 6344—
生成物1-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazineHCID 1498056472%

反応手順

To a suspension of 4-methoxyphenylhydrazine hydrochloride (41 g, 230 mmol) in methylene chloride (1000 ml) under nitrogen were added diisopropylamine (79.8 g, 612 mmol), 4-chlorobenzylchloride (40.25 g, 250 mmol) and tetrabutylammonium bromide (22.8 g, 70 mmol). The resulting mixture was stirred at ambient temperature for 48 hours. The reaction mixture was then washed with water, and brine, dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by column chromatography (silica gel, 2.5% methanol in methylene chloride) followed by washing of the solid with 10% ethyl ether in hexane and drying in vacuo to provide 43.5 g of 1-(4-chlorobenzyl)-1-(4methoxyphenyl)hydrazine, mp. 55° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420282
出典データセットuspto-grants-1995_05
ORD IDord-d8ce271105e24509955cfcff1c341e5f
出典メモuspto-grants-1995_05