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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66761Generated: October 25, 2026

1,2-Dichlorobenzene → 2-((2,4-Dichloroanilino)methyl)-2-imidazoline p-toluenesulfonate

https://huagongshe.com/reaction/66761

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichlorobenzeneHCID 7239—
Reactant1,2-Ethanediamine, 4-methylbenzenesulfonate (1:?)HCID 225030—
Reactant(2,4-Dichloroanilino)acetonitrileHCID 12832563—
SolventDichloromethaneHCID 6344—
Product2-((2,4-Dichloroanilino)methyl)-2-imidazoline p-toluenesulfonateHCID 2052906684.1%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04343810
Source datasetuspto-grants-1982_08
ORD IDord-52e50704029f482f85e1790684a02ab5
Source noteuspto-grants-1982_08