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HRID 66762作成日:2026年10月25日

Dichloromethane → 2-((2,4-Dichloroanilino)methyl)-2-imidazoline

https://huagongshe.com/reaction/66762

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物2-((2,4-Dichloroanilino)methyl)-2-imidazoline p-toluenesulfonateHCID 20529066—
溶媒WaterHCID 962—
生成物2-((2,4-Dichloroanilino)methyl)-2-imidazolineHCID 20529067—

反応手順

A mixture of 21.5 grams (g) of 2,4-dichloroanilinoacetonitrile, 23.3 g of ethylenediamine p-toluenesulfonate and 75 milliliters (ml) of 1,2-dichlorobenzene was heated with stirring in a round-bottomed three-necked flask at from about 140°-170° C. for about 70 minutes under a small flow of nitrogen. The reaction mixture was cooled and then diluted with methylene chloride. The mixture was cooled and then filtered, which gave 35.1 g of 2-((2,4-dichloroanilino)methyl)-2-imidazoline p-toluenesulfonate as white crystals. The p-toluenesulfonate salt was slurried in water and CH2Cl2 and then basified. The CH2Cl2 layer was separated and the remaining aqueous portion extracted with CH2Cl2 and then CHCl3. The extracts were combined, treated with diatomaceous earth and activated charcoal, and then filtered. Concentrating the filtrate to dryness, left 17.0 g of crystals. Recrystallization from ethylene dichloride gave 14.0 g of purified 2-((2,4-dichloroanilino)methyl)-2-imidazoline as white crystals, having a melting point (m.p.) of 154°-156° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04343810
出典データセットuspto-grants-1982_08
ORD IDord-319ebae7e3ee41ed996af7686be1c5bb
出典メモuspto-grants-1982_08