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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833177Generated: October 25, 2026

Iodine → [1-(4-Benzyloxy-3-methoxy-phenyl)-2-(3-ethoxy-phenyl)-ethyl]-(2,2-dimethoxy-ethyl)-amine

https://huagongshe.com/reaction/1833177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
Reactant(4-Benzyloxy-3-methoxy-benzylidene)-(2,2-dimethoxy-ethyl)-amineHCID 22048289—
Reactant1-(Chloromethyl)-3-ethoxybenzeneHCID 22048372—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product[1-(4-Benzyloxy-3-methoxy-phenyl)-2-(3-ethoxy-phenyl)-ethyl]-(2,2-dimethoxy-ethyl)-amineHCID 22048411—

Reaction Steps

3-Ethoxybenzylchloride (13.6 g, 80 mmol) was dissolved in diethyl ether (100 mL) and magnesium metal (2.04 g, 84 mmol) was added without stirring. Several crystals of iodine were added to the magnesium “pile”. When the reaction begins, stirring is started and external cooling is applied as necessary to maintain gentle refluxing. Once the initial reaction was complete, the mixture was refluxed for 1 h to complete the reaction. The resulting gray/green mixture was cooled in an ice-bath and (4-benzyloxy-3-methoxy-benzylidene)-(2,2-dimethoxy-ethyl)-amine (13.2 g, 40 mmol) in diethyl ether (60 mL) was added dropwise (a precipitate forms with each drop). After addition was complete, the resulting suspension was heated at reflux for 2 hours. The mixture was cooled in an ice-bath and saturated aqueous ammonium chloride solution (100 mL) was carefully added dropwise. The mixture was stirred at 0° C. for 15 minutes and then room temperature for 1 h. Water (80 mL) was added, and the mixture was filtered. The organic layer was separated, washed with water (50 mL), saturated aqueous sodium chloride solution (40 mL), dried over magnesium sulfate, filtered and concentrated in vacuo to afford [1-(4-benzyloxy-3-methoxy-phenyl)-2-(3-ethoxy-phenyl)-ethyl]-(2,2-dimethoxy-ethyl)-amine as a light tan solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067529B2
Source datasetuspto-grants-2006_06
ORD IDord-54eae1dfafe146d384ba6f7be8f163a5
Source noteuspto-grants-2006_06