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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404976Generated: October 29, 2026

O-Methyltyramine → N-[2-(4-methoxyphenyl)ethyl]cyclopentanamine

https://huagongshe.com/reaction/404976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-MethyltyramineHCID 4657—
ReactantIodocyclopentaneHCID 73784—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductN-[2-(4-methoxyphenyl)ethyl]cyclopentanamineHCID 28445893194.7%

Reaction Steps

4-Methoxyphenethyl amine (0.8 mL, 6 mmol), and cyclopentyl iodide (0.22 mL, 2 mmol) in CH3CN (5 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-(4-methoxyphenethyl)cyclopentanamine (0.854 g, 65%) was obtained as a colorless liquid which solidified upon standing. 1H NMR (400 MHz, CDCl3): δ 8.49 (s, 1H), 7.10 (d, 2H, J=8.6 Hz), 6.78 (d, 2H, J=8.6 Hz), 3.74 (s, 3H), 3.69-3.65 (m, 1H), 3.08-3.07 (m, 4H), 1.84-1.83 (m, 2H), 1.82-1.81 (m, 2H), 1.66-1.56 (m, 4H). 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-4cc6a1e5da5645198fa1631f24f53442
Source noteuspto-grants-2014_06