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HRID 1833187作成日:2026年10月25日

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

https://huagongshe.com/reaction/1833187

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Ammonium ChlorideHCID 25517—
反応物MagnesiumHCID 5462224—
反応物(4-Benzyloxy-3-methoxy-benzylidene)-(2,2-dimethoxy-ethyl)-amineHCID 22048289—
反応物1-(Chloromethyl)-3-ethoxybenzeneHCID 22048372—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物[1-(4-Benzyloxy-3-methoxy-phenyl)-2-(3-ethoxy-phenyl)-ethyl]-(2,2-dimethoxy-ethyl)-amineHCID 22048411—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07067529B2
出典データセットuspto-grants-2006_06
ORD IDord-8696af162b5343ca8678b410e482f42b
出典メモuspto-grants-2006_06