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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | N-Methylhomoveratrylamine | HCID 77039 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-((3,4-Dimethoxyphenethyl)(methyl)amino)ethanol | HCID 14407318 | 37.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06057358 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-ca10af87355c46d194c955e99b2c40d1 |
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| Source note | uspto-grants-2000_05 |
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