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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297700Generated: October 31, 2026

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

https://huagongshe.com/reaction/2297700

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 numberUS06492370B1
Source datasetuspto-grants-2002_12
ORD IDord-0661d0e8c8da47209f1e8e5289cabb4e
Source noteuspto-grants-2002_12