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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323259생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/323259

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물2-PyrrolidoneHCID 12025—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물3,4,5-Trimethoxybenzyl MesylateHCID 18464591—
용매TetrahydrofuranHCID 8028—
생성물1-(3,4,5-Trimethoxybenzyl)-2-oxopyrrolidineHCID 18464662—

반응 조건

온도-78 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211199B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-a3c903c1840e48eaab629b6bd9865ccc
출처 메모uspto-grants-2001_04