HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 396590Erstellt: 25. Oktober 2026
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/396590
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Edukt | 5-Benzo[b]thiophen-2-yl-2,4-dimethoxy-benzaldehyde | HCID 16115916 | — |
| Edukt | 1-(4-((tert-Butyldimethylsilyl)oxy)-3,5-dimethoxyphenyl)ethanone | HCID 22025593 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-[5-(Benzo[b]thien-2-yl)2,4-dimethoxyphenyl]-1-(4-tert-butyldimethylsiloxy-3,5-dimethoxyphenyl)-2-propen-1-one | HCID 69620906 | 20% |
Reaktionsschritte
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-ter-butyldimethylsiloxy-3,5-dimethoxyphenyl)-2-propen-1-one as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06608101B1 |
|---|
| Quelldatensatz | uspto-grants-2003_08 |
|---|
| ORD ID | ord-86a61a678e534cdb831ed449571f3667 |
|---|
| Quellennotiz | uspto-grants-2003_08 |
|---|