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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323493생성일: 2026년 10월 27일

Tetrahydrofuran → 1-(3,4,5-Trimethoxybenzyl)-3-(3-(t-butyldimethylsilyloxy)propyl)-2-oxopyrrolidine

https://huagongshe.com/reaction/323493

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Tert-butyl-(3-iodopropoxy)-dimethylsilaneHCID 11022956—
반응물1-(3,4,5-Trimethoxybenzyl)-2-oxopyrrolidineHCID 18464662—
반응물CID 53628100HCID 178418400—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물1-(3,4,5-Trimethoxybenzyl)-3-(3-(t-butyldimethylsilyloxy)propyl)-2-oxopyrrolidineHCID 22009451—

반응 조건

온도-78 °C

반응 단계

Combine 1-(3,4,5-trimethoxybenzyl)-2-oxopyrrolidine (0.84 g, 3.16 mmol) and tetrahydrofuran (10 mL). Cool to −78° C. using a dry-ice/acetone bath. Add a solution of sec-butyl lithium (2.56 mL, 1.3 M in hexane, 3.33 mmol). After 30 minutes, add 3-(t-butyldimethylsilyloxy)propyl iodide (1.0 g, 3.33 mmol). After the addition is complete, warm to ambient temperature. After 2 hours, add water and extract three 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211199B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-cc292f7d6f9a45dc8e9ce1f2816341bd
출처 메모uspto-grants-2001_04