Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404981Generated: October 31, 2026

Iodocyclopentane → HCID 28814460, compound

https://huagongshe.com/reaction/404981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodocyclopentaneHCID 73784—
Reactant3-MethoxyphenethylamineHCID 74866—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 28814460HCID 2881446066.1%

Reaction Steps

3-Methoxyphenethylamine (4.5 mL, 30 mmol), and cyclopentyl iodide (1.15 mL, 10 mmol) in CH3CN (15 mL) were irradiated for 10 min in a microwave at 110° C. After cooling to room temperature the mixture was diluted with CH2Cl2 and washed with NaHCO3 solution. The organic layer was dried over anhydrous Na2SO4 and evaporated in vacuo. The crude product was purified by silica gel chromatography using hexane as eluent and the product N-(3-methoxyphenethyl)cyclopentanamine (1.45 g, 66%) was obtained as a colorless liquid which solidified upon standing. 1H NMR (400 MHz, CDCl3): δ 8.48 (s, 1H), 7.20 (t, 1H, J=8.0 Hz), 6.79-6.73 (overlapping doublets and singlet, 3H), 3.74 (s, 3H), 3.44-3.39 (m, 1H), 3.38-3.11 (m, 4H), 1.84-1.83 (m, 2H), 1.82-1.81 (m, 4H), 1.66-1.56 (m, 2H). LC-MS (ESI) Calcd for: C14H21NO [M+H]+: 220.16. Found: 220.00.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748632B2
Source datasetuspto-grants-2014_06
ORD IDord-ed5359e04036438499f2e175b40507e3
Source noteuspto-grants-2014_06