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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66727Generated: October 25, 2026

Methane → HCID 28918746, compound

https://huagongshe.com/reaction/66727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
Reactant1,2-DichlorobenzeneHCID 7239—
Reactant1,2-Ethanediamine, 4-methylbenzenesulfonate (1:?)HCID 225030—
Reactant4-Chloro-m-tolyloxyacetonitrileHCID 43242589—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 28918746HCID 2891874632.7%

Reaction Steps

A mixture of 36.3 g of 4-chloro-m-tolyloxyacetonitrile, 46.6 g of ethylenediamine p-toluenesulfonate and 150 ml of 1,2-dichlorobenzene was heated with stirring in a 500 ml round-bottomed three-necked flask at reflux under a small flow of nitrogen for 1.5 hours, essentially as described in U.S. Pat. No. 3,449,356. The reaction mixture was cooled, diluted with methylene chloride and the solids filtered off. The solids were slurried in water and then basified with 5 normal (N) sodium hydroxide and then filtered. The solids were washed well with water and dried to obtain 42.0 g of the crude product, m.p. 91°-95° C. A 19.5 g portion of the crude product was put in solution in approximately 150 ml of boiling toluene, treated with activated charcoal and filtered. The filtrate was cooled and then filtered, which gave 14.7 g of purified 2-(((4-chloro-m-tolyl)oxy)methyl)-2-imidazoline, m.p. 90°-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04343809
Source datasetuspto-grants-1982_08
ORD IDord-2821cd02ba4e44d9b486448b99a06b08
Source noteuspto-grants-1982_08