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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057375Generated: October 31, 2026

Benzyltrimethylammonium hydroxide → HCID 70546733, compound

https://huagongshe.com/reaction/2057375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
ReactantN-(2,6-Dichlorophenyl)-N-(prop-2-yn-1-yl)-4,5-dihydro-1H-imidazol-2-amineHCID 20332207—
CatalystEthanolHCID 702—
ProductHCID 70546733HCID 7054673318.7%

Reaction Steps

A mixture consisting of 5.4 gm of 2-[N-(2,6-dichloro-phenyl)-N-propargyl-amino]-2-imidazoline and 40 ml of ethanol containing 5 drops of trimethylbenzyl ammonium hydroxide was refluxed for five hours, while stirring. Thereafter, the ethanol was evaporated in vacuo, and the residue was dissolved in dilute hydrochloric acid. The resulting solution was fractionally extracted with ether at stepwisely increasing pH-values (addition of 2 N sodium hydroxide). The thin-layer chromatographically uniform ethereal fractions having a pH of 9 or more were combined, dried over magnesium sulfate, and the ether was evaporated in vacuo, leaving 1 gm (18.7% of theory) of 7-(2,6-dichloro-phenyl)-2,3-dihydro-5-methyl-imidazo[1,2-α]imidazole, m.p. 113°-117° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04210659
Source datasetuspto-grants-1980_07
ORD IDord-03058b514d05496faa348475546a3566
Source noteuspto-grants-1980_07