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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581810Generated: November 2, 2026

Sodium Iodide → N-(t-butoxycarbonyl)-N'-cyclohexyl-N'-methylethylenediamine

https://huagongshe.com/reaction/1581810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantN-MethylcyclohexylamineHCID 7514—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl N-(2-bromoethyl)carbamateHCID 4103526—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-(t-butoxycarbonyl)-N'-cyclohexyl-N'-methylethylenediamineHCID 2272289872%

Reaction Steps

To a solution of N-(t-butoxycarbonyl)-2-bromoethylamine (1.0 g) in anhydrous dimethylformamide (15 ml) are added N-methylcyclohexylamine (0.64 ml), anhydrous potassium carbonate (0.9 g) and sodium iodide (2.0 g), and the mixture is stirred at room temperature for three days. Water is added to the reaction mixture, and the whole is extracted with ether. The organic layer is washed with a 10% aqueous sodium hydrogencarbonate solution, water and saturated brine successively, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography to give 0.82 g (72%) of N-(t-butoxycarbonyl)-N′-cyclohexyl-N′-methylethylenediamine as oily matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730784B2
Source datasetuspto-grants-2004_05
ORD IDord-685a394c721849cdba65bf1296958970
Source noteuspto-grants-2004_05