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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410143Generated: October 29, 2026

Potassium Iodide → 3-chloro-N-[(1R)-1-(naphthalen-1-yl)ethyl]prop-2-en-1-amine hydrochloride

https://huagongshe.com/reaction/410143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-DichloropropeneHCID 24883—
Reactant(+)-1-(1-Naphthyl)ethylamineHCID 2724264—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-chloro-N-[(1R)-1-(naphthalen-1-yl)ethyl]prop-2-en-1-amine hydrochlorideHCID 86674601—

Reaction Steps

Potassium carbonate (161.2 g) and potassium iodide (5 g) were added to a solution of (R)-1(1-naphthyl)ethylamine (100 g) and 1,3-dichloropropene (97.3 g) in acetonitrile (1 L) at room temperature. The reaction mixture was refluxed at 80° C. to 85° C. for 4 hours. After the completion of the reaction, the mixture was cooled to room temperature and de-ionized water (500 mL) was added. The solution was stirred for 15 minutes and layers were separated. The organic layer was concentrated under vacuum at 55° C. to 60° C. till about 100 to 150 mL of residue was left. Toluene (500 mL) was added to the residue and the organic layer was washed twice with de-ionized water (2×250 mL). The organic layer was concentrated under vacuum at 55° C. to 60° C. Isopropyl alcohol was added to the residue and stirred for 10 minutes at room temperature. The pH of the solution was adjusted to 0.5 to 1.0 using concentrated hydrochloric acid (35 mL) and stirred for one hour at room temperature. The solid was filtered, washed with isopropyl alcohol (2×100 mL) and dried under vacuum at 45° C. to 50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759586B2
Source datasetuspto-grants-2014_06
ORD IDord-d280ecfc7458440683e57b6c63168e3d
Source noteuspto-grants-2014_06