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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305306Generated: November 1, 2026

Methyl iodide → Hydrogen iodide

https://huagongshe.com/reaction/2305306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 73840649HCID 73840649—
SolventMethanolHCID 887—
ProductHydrogen iodideHCID 24841—
ProductHCID 54448851HCID 54448851—

Reaction Steps

5 g of 1-benzylideneamino-imidazolidine-2-thion are suspended in 40 ml of methanol and treated with 1.7 ml of methyliodide. The mixture obtained is refluxed for ca. one hour and the solvent is evaporated off. 1-Benzylideneamino-2-methylthio-4,5-dihydro-1H-imidazole in the form of a hydroiodide is obtained in solid form, to which 120 ml of water and 70 ml of an anion exchange resin in chloride form (Amberlite IRA-400 (Cl)R) are added. The mixture is stirred for ca. 2 hours at room temperature, filtrated and lyophilized. 1-Benzylideneamino-2-methylthio-4,5-dihydro-1H-imidazole in the form of a hydrochloride is obtained in the form of a lyophilisate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06440957B1
Source datasetuspto-grants-2002_08
ORD IDord-b515248b040f428f877b420dff66edaf
Source noteuspto-grants-2002_08