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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106862Generated: October 27, 2026

Potassium Iodide → 2-((3,4-Dimethoxyphenethyl)(methyl)amino)ethanol

https://huagongshe.com/reaction/1106862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2-BromoethanolHCID 10898—
ReactantN-MethylhomoveratrylamineHCID 77039—
SolventDimethylformamideHCID 6228—
Product2-((3,4-Dimethoxyphenethyl)(methyl)amino)ethanolHCID 1440731837.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-(3,4-Dimethoxyphenyl)-N-methylethylamine (2.77 ml, 0.015 mol) and 2-bromoethanol (1.13 ml, 0.015 mol) were dissolved in N,N-dimethylformamide (10 ml). To the resulting solution, potassium iodide (2.45 g, 0.015 mol) was added, followed by stirring at 80° C. for 1.5 h. The reaction mixture was cooled to room temperature and, thereafter the solvent was evaporated under vacuum; after adding a saturated aqueous solution of sodium bicarbonate, three extractions were conducted with ethyl acetate. The organic layers were combined, dried with sodium sulfate and concentrated under vacuum. The residue was purified by being subjected to column chromatography on silica gel using a 9:1 solvent system of chloroform and methanol as an eluent and the fractions containing the end product were collected and the solvent was evaporated under vacuum, followed by drying to yield the end compound 2-[N-(3,4-dimethoxyphenethyl)-N-methylamino]ethanol (1.35 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057358
Source datasetuspto-grants-2000_05
ORD IDord-ca10af87355c46d194c955e99b2c40d1
Source noteuspto-grants-2000_05