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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660527Generated: November 3, 2026

Iodoethane → HCID 86738182, compound

https://huagongshe.com/reaction/1660527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantHCID 11010529HCID 11010529—
SolventMethanolHCID 887—
ProductHCID 86738182HCID 86738182—

Reaction Steps

25 ml of methanol and 1.85 g of ethyl iodide are added to 2.5 g of DL-trans-4,5-diphenyl-imidazolidine-2-thione and the mixture is refluxed for 15 hours. A further 0.4 g of ethyl iodide is then added and the mixture is refluxed for a further 5 hours. It is then evaporated to dryness. DL-trans-2-Ethylthio-4,5-diphenyl-imidazoline hydroiodide is obtained. In order to convert it to the base, this hydroiodide is suspended in 100 ml of ethyl acetate and 100 ml of water, the suspension is rendered alkaline with concentrated aqueous ammonia solution and the organic phase is separated off, dried over sodium sulfate and evaporated. DL-trans-2-Ethylthio-4,5-diphenyl-imidazoline with a melting point of 130°-132° is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04308277
Source datasetuspto-grants-1981_12
ORD IDord-923ce70f04064f9c8e862be1821fab07
Source noteuspto-grants-1981_12