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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220166Generated: October 30, 2026

Ethylenediamine → 1-(2-Imidazolin-2-YL)-6-methoxy-5-methylindane

https://huagongshe.com/reaction/2220166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant6-Methoxy-5-methyl-2,3-dihydro-1H-indene-1-carbonitrileHCID 45091405—
SolventDichloromethaneHCID 6344—
SolventPotassium CarbonateHCID 11430—
Product1-(2-Imidazolin-2-YL)-6-methoxy-5-methylindaneHCID 1170139170.1%

Reaction Steps

A mixture of 2.4 grams (0.013 mole) of 6-methoxy-5-methylindanecarbonitrile (iv) and 11.2 grams (0.045 mole) of the ethylenediamine salt of p-toluenesulfonic acid was stirred and heated to about 140° C.-160° C. where it was maintained for about 4.5 hours. The reaction mixture was then cooled to ambient temperature and dissolved in a mixture of aqueous 5% potassium carbonate and methylene chloride. The organic layer was removed, and the aqueous layer was extracted with two portions of methylene chloride. The combined extracts and organic layer were washed with one portion of aqueous 5% potassium carbonate. The organic layer was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to a solid residue. The residue was purified by column chromatography on Grade II basic alumina (3% water) using mixtures of methylene chloride and methanol as an eluant. The appropriate fractions of eluate were combined and concentrated under reduced pressure, yielding about 2.1 grams of subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417057B2
Source datasetuspto-grants-2008_08
ORD IDord-e8550e68e3c14b838d51b85796fb18c5
Source noteuspto-grants-2008_08