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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | 5-Benzo[b]thiophen-2-yl-2,4-dimethoxy-benzaldehyde | HCID 16115916 | — |
| 반응물 | 1-(4-((tert-Butyldimethylsilyl)oxy)-3,5-dimethoxyphenyl)ethanone | HCID 22025593 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-[5-(Benzo[b]thien-2-yl)2,4-dimethoxyphenyl]-1-(4-tert-butyldimethylsiloxy-3,5-dimethoxyphenyl)-2-propen-1-one | HCID 69620906 | 20% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07078431B2 |
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| 출처 데이터셋 | uspto-grants-2006_07 |
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| ORD ID | ord-7211d0c745c549738a94877ba304ff6d |
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| 출처 메모 | uspto-grants-2006_07 |
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