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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323494생성일: 2026년 10월 25일

Tetrahydrofuran → 1-(3,4,5-Trimethoxybenzyl)-3-(4-fluorophenylmethyl)-3-(3-t-butyldimethylsilyloxypropyl)-2-oxopyrrolidine

https://huagongshe.com/reaction/323494

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물4-Fluorobenzyl bromideHCID 68021—
반응물1-(3,4,5-Trimethoxybenzyl)-3-(3-(t-butyldimethylsilyloxy)propyl)-2-oxopyrrolidineHCID 22009451—
반응물CID 53628100HCID 178418400—
용매WaterHCID 962—
용매Ethyl acetate hexaneHCID 21226206—
생성물1-(3,4,5-Trimethoxybenzyl)-3-(4-fluorophenylmethyl)-3-(3-t-butyldimethylsilyloxypropyl)-2-oxopyrrolidineHCID 18464618—

반응 조건

온도-78 °C

반응 단계

Combine 1-(3,4,5-trimethoxybenzyl)-3-(3-(t-butyldimethylsilyloxy)propyl)-2-oxopyrrolidine (0.71 g, 1.62 mmol) and tetrahydrofuran (10 mL). Cool to −78° C. using a dry-ice/acetone bath. Add a solution of sec-butyl lithium (1.37 mL, 1.3 M in hexane, 1.78 mmol). After 30 minutes, add 4-fluorobenzyl bromide (0.34 g, 1.78 mmol). After 15 minutes, warm slowly to ambient temperature. After 12 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 1/1 ethyl acetate/hexane to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211199B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-b96792c495954cdcacfd5987bd81e23e
출처 메모uspto-grants-2001_04