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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1577140생성일: 2026년 10월 27일

2-Chloroaniline → Imidazolidine, 2-(2-chlorophenylimino)-

https://huagongshe.com/reaction/1577140

반응식

참여 물질

역할이름HCID투입량
반응물2-ChloroanilineHCID 7240—
반응물Sodium HydroxideHCID 14798—
반응물2-Chloroimidazoline sulfateHCID 12503398—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물Imidazolidine, 2-(2-chlorophenylimino)-HCID 13834248%

반응 단계

To 2-chloroimidazoline bisulfate (60.0 g, 300 mmoles) in methanol (600 ml) and water (150 ml) is added with stirring 2-chloroaniline (81.1 g, 67 ml, 636 mmoles). The heterogeneous mixture is stirred at ambient temperature overnight. After 20 hours the mixture is poured into ice water, made strongly alkaline with sodium hydroxide and extracted with dichloromethane twice. The organic extracts are washed once with water and once with saturated sodium chloride solution and then extracted with 2 N acetic acid (2×1 liter). The combined acid extracts are backwashed with dichloromethane, made strongly alkaline with sodium hydroxide, and once again extracted with dichloromethane twice. The dichloromethane extracts are combined, washed with water and then sodium chloride solution and finally dried and evaporated in vacuo. The solid residue (31 g) is dissolved in hot toluene, filtered, and diluted with hexane (total volume 3 liters). Colorless crystals separate which are filtered, washed with hexane and air-dried, to give 28.2 g of 2-(2-chlorophenylimino)imidazolidine, m.p. 133°-134° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04287201
출처 데이터셋uspto-grants-1981_09
ORD IDord-2f73aa793ac34c45ae2ae5c5f10b475b
출처 메모uspto-grants-1981_09