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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519696Generated: November 4, 2026

Cyclopropylamine → N-[1-(4-iodophenyl)ethyl]cyclopropanamine

https://huagongshe.com/reaction/1519696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
Reactant1-(4-Iodophenyl)ethan-1-oneHCID 72869—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
ProductN-[1-(4-iodophenyl)ethyl]cyclopropanamineHCID 4375463195%

Reaction Steps

Cyclopropylamine (0.85 g), acetic acid (0.89 g), and sodium triacetoxyborohydride (3.2 g) were added to a chloroform (20 mL) solution of 1-(4-iodophenyl)ethanone (1.2 g), and the mixture was stirred in a nitrogen atmosphere for 24 hours at room temperature. A saturated aqueous solution of sodium hydrogen carbonate was added to the reaction mixture, and then the mixture was extracted with chloroform. Then, the organic layer was washed with brine, and dried over anhydrous magnesium sulfate. Then, the desiccant was filtered out, and the solvent was distilled off under reduced pressure. The resulting residue was purified by OH type silica gel chromatography (hexane/ethyl acetate=80/20) to obtain N-[1-(4-iodophenyl)ethyl]cyclopropylamine (colorless oil) (1.3 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073821B2
Source datasetuspto-grants-2015_07
ORD IDord-0238b18d452b415d951d8eec4ddc74d2
Source noteuspto-grants-2015_07