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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66766Generated: October 25, 2026

Methane → HCID 20529046, compound

https://huagongshe.com/reaction/66766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantEthanolHCID 702—
Reactant1,2-Ethanediamine, 4-methylbenzenesulfonate (1:?)HCID 225030—
Reactant4-(Cyanomethoxy)benzonitrileHCID 20529061—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductHCID 20529046HCID 20529046—

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of 15.8 g of 4-cyanophenoxyacetonitrile and 23.3 g of ethylenediamine p-toluenesulfonate in 50 ml of 1,2-dichlorobenzene was heated at from about 130°-145° C. for about an hour. After reaction the mixture was cooled, diluted with CH2Cl2 and filtered to obtain the crude product. The crude product was dissolved in boiling absolute ethanol, treated with activated charcoal and filtered through a fluted paper. The filtrate was cooled to 5° C. for 1.5 hours and the crystals which formed removed by filtering. After drying in a vacuum oven, off-white crystals were obtained having a melting point of 190°-192° C. The off-white crystals were put in solution in 200 ml of boiling water and treated with activated charcoal and filtered. The filtrate was cooled to 5° C. for 1 hour and the crystals which formed removed by filtration. Upon drying, the product 2-((4-cyanophenoxy)methyl)-2-imidazoline p-toluenesulfonate was obtained as white crystals, m.p. 196°-198° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04343808
Source datasetuspto-grants-1982_08
ORD IDord-eb7a0cf14e554f1c8b942e4242ebdfe8
Source noteuspto-grants-1982_08