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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 66762Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/66762

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt2-((2,4-Dichloroanilino)methyl)-2-imidazoline p-toluenesulfonateHCID 20529066—
LösungsmittelWaterHCID 962—
Produkt2-((2,4-Dichloroanilino)methyl)-2-imidazolineHCID 20529067—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04343810
Quelldatensatzuspto-grants-1982_08
ORD IDord-319ebae7e3ee41ed996af7686be1c5bb
Quellennotizuspto-grants-1982_08