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HRID 1011558作成日:2026年10月25日

Hydrochloric Acid → 1-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazine hydrochloride

https://huagongshe.com/reaction/1011558

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物1-Chloro-4-(chloromethyl)benzeneHCID 7723—
反応物DiisopropylethylamineHCID 81531—
反応物4-Methoxyphenylhydrazine hydrochlorideHCID 2723904—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
溶媒1,4-DioxaneHCID 31275—
生成物1-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazine hydrochlorideHCID 18947569—

反応手順

A solution of 4-Methoxyphenylhydrazine hydrochloride (10.0 g, 57.3 mmol), 4-chlorobenzylchloride (9.2 g, 57.2 mmol), tetrabutylammonium bromide (3.7 g, 11.5 mmol), and diisopropylethylamine (2 mL, 115 mmol) in CH2Cl2 (250 mL) was stirred at room temperature for several days. The reaction mixture was diluted with water and the organic layer was dried over MgSO4, filtered, and concentrated. The residue was taken up in toluene (200 mL) and diethyl ether (100 mL), and 1 equivalent of 4N HCl in dioxane was added at 0° C. The mixture was stirred at room temperature for 2 hours, and then evaporated to dryness to give the desired product (C-1; X═Cl) as a purple solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07977359B2
出典データセットuspto-grants-2011_07
ORD IDord-a227c940778f4a3bb3ccab8d39738ea0
出典メモuspto-grants-2011_07