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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37443생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/37443

반응식

참여 물질

역할이름HCID투입량
반응물1-Chloro-4-(chloromethyl)benzeneHCID 7723—
반응물DiisopropylamineHCID 7912—
반응물4-Methoxyphenylhydrazine hydrochlorideHCID 2723904—
촉매Tetrabutylammonium BromideHCID 74236—
용매DichloromethaneHCID 6344—
생성물1-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazineHCID 1498056472%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420282
출처 데이터셋uspto-grants-1995_05
ORD IDord-d8ce271105e24509955cfcff1c341e5f
출처 메모uspto-grants-1995_05