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HRID 323259作成日:2026年10月25日

Ethyl Acetate → 1-(3,4,5-Trimethoxybenzyl)-2-oxopyrrolidine

https://huagongshe.com/reaction/323259

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物2-PyrrolidoneHCID 12025—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
反応物3,4,5-Trimethoxybenzyl MesylateHCID 18464591—
溶媒TetrahydrofuranHCID 8028—
生成物1-(3,4,5-Trimethoxybenzyl)-2-oxopyrrolidineHCID 18464662—

反応条件

温度-78 °C

反応手順

Combine 2-pyrrolidinone (2.85 g, 33.5 mmol) and tetrahydrofuran (70 mL). Cool to −78° C. using a dry-ice/acetone bath. Add a solution of potassium bis(trimethylsilyl)amide (67 mL, 0.5 M in toluene, 33.5 mol). After 45 minutes, add a solution of 3,4,5-trimethoxybenzyl mesylate (8.8 g, 32.02 mmol) in tetrahydrofuran (60 mL). After the addition of 3,4,5-trimethoxybenzyl mesylate is complete, heat to reflux. After 18 hours, cool the reaction mixture and partition between water and ethyl acetate. Separate the aqueous layer and extract 4 times with ethyl acetate. Dry the combined organic layers over Na2SO4, filter, and concentrate in vacuo to obtain a residue. Chromatograph the residue on silica gel eluting with ethyl acetate to give the title compound: Rf=0.35 (silica gel, ethyl acetate).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211199B1
出典データセットuspto-grants-2001_04
ORD IDord-a3c903c1840e48eaab629b6bd9865ccc
出典メモuspto-grants-2001_04