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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647843Generated: November 1, 2026

Sodium Iodide → HCID 22355248, compound

https://huagongshe.com/reaction/1647843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPropylamineHCID 7852—
ReactantPotassium CarbonateHCID 11430—
ReactantToluene-4-sulfonic acid tetrahydro-furan-3-ylmethyl esterHCID 15335290—
SolventEthanolHCID 702—
ProductHCID 22355248HCID 22355248—

Reaction Steps

A mixture comprising 3.00 g of (tetrahydro-3-furanyl)methyl tosylate, 0.20 g of sodium iodide, 3.50 g of potassium carbonate, 4.00 g of propylamine and 30 ml of ethanol was refluxed for 8 hours. After separation of insoluble matters by filtration, the reaction fluid was concentrated under a reduced pressure to obtain crude N-{(tetrahydro-3-furanyl)methyl}propylamine. To this were added 1.90 g of 1,1-bis(methylthio)-2-nitroethylene and 16 ml of acetonitrile. The resulting mixture was refluxed for 4 hours. The reaction fluid was concentrated under a reduced pressure, and purified by silica gel column chromatograpy (eluent: ethyl acetate/hexane=1/2) to obtain 1.00 g of 1-[N-{(tetrahydro-3-furanyl)methyl}-N-propylamino]-1-methylthio-2-nitroethylene. A mixture comprising 0.25 g of the 1-[N-{(tetrahydro-3-furanyl)methyl}-N-propylamino]-1-methylthio-2-nitroethylene obtained above and 3 ml of 40% methylamine in methanol solution was stirred for 40 minutes at room temperature. The reaction fluid was concentrated under a reduced pressure, and purified by silica gel column chromatography (eluent: ethyl acetate/methanol=7/1) to obtain 0.22 g of 1-[N-{(tetrahydro-3-furanyl)methyl}propylamino]-1-methylamino-2-nitroethylene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434181
Source datasetuspto-grants-1995_07
ORD IDord-0a3cc9bfdf7c4a0caee1dcf0e90aeda0
Source noteuspto-grants-1995_07