戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1928637作成日:2026年10月25日

Sodium Iodide → (2R)-1-[3-(4-iodophenoxy)propyl]-2-methylpyrrolidine

https://huagongshe.com/reaction/1928637

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Potassium CarbonateHCID 11430—
反応物(R)-2-MethylpyrrolidineHCID 641544—
反応物1-(3-Chloropropoxy)-4-iodobenzeneHCID 15895520—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物(2R)-1-[3-(4-iodophenoxy)propyl]-2-methylpyrrolidineHCID 57675747—

反応条件

温度100 °C

反応手順

A suspension of 1-(3-chloropropoxy)-4-iodobenzene obtained in Example 1-(1) (2.79 g), (R)-2-methylpyrrolidine (0.961 g), sodium iodide (0.282 g) and potassium carbonate (2.60 g) in acetonitrile (2.8 mL) was stirred in a sealed tube at 100° C. for 5 hours. The reaction mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate. The organic layer was washed with water and brine, dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluting solvent: n-hexane:ethyl acetate=10:1) to give the titled compound (3.27 g) as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08183387B2
出典データセットuspto-grants-2012_05
ORD IDord-8fe2dd441f9b4730ad763dcbf7990218
出典メモuspto-grants-2012_05