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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1792974생성일: 2026년 10월 27일

Lithium diisopropylamide → 3-[5-(Benzo[b]thien-2-yl)2,4-dimethoxyphenyl]-1-(4-tert-butyldimethylsiloxy-3,5-dimethoxyphenyl)-2-propen-1-one

https://huagongshe.com/reaction/1792974

반응식

참여 물질

역할이름HCID투입량
반응물Lithium diisopropylamideHCID 2724682—
반응물5-Benzo[b]thiophen-2-yl-2,4-dimethoxy-benzaldehydeHCID 16115916—
반응물1-(4-((tert-Butyldimethylsilyl)oxy)-3,5-dimethoxyphenyl)ethanoneHCID 22025593—
용매TetrahydrofuranHCID 8028—
생성물3-[5-(Benzo[b]thien-2-yl)2,4-dimethoxyphenyl]-1-(4-tert-butyldimethylsiloxy-3,5-dimethoxyphenyl)-2-propen-1-oneHCID 6962090620%

반응 단계

Ex-59B: To a solution of 3′,5′-dimethoxy-4′-(tert-butyldimethylsiloxy)acetophenone, from Ex-59A (0.5 g, 1.6 mmol) in tetrahydrofuran (10 mL) chilled with ice/water was added lithium diisopropylamide (2 M, 0.8 mL, 1.6 mmol). The mixture was stirred for 20 minutes while chilled. Then 5-(benzo[b]thien-2-yl)-2,4-dimethoxybenzaldehyde, from Ex-6A,(0.48 g, 1.6 mmol) in tetrahydrofuran (6 mL) was added, and the mixture was stirred at room temperature for 2 hours. Upon quenching with water, the mixture was extracted with dichloromethane. The organic phase was dried and evaporated. Crystallization from ethanol gave 0.19 g (20%) of the desired 3-[5-(benzo[b]thien-2-yl)2,4-dimethoxyphenyl]-1-(4-tert-butyldimethylsiloxy-3,5-dimethoxyphenyl)-2-propen-1-one as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07078431B2
출처 데이터셋uspto-grants-2006_07
ORD IDord-7211d0c745c549738a94877ba304ff6d
출처 메모uspto-grants-2006_07