HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 731168Erstellt: 25. Oktober 2026
Ethyl trimethylsilylacetate → Ethyl 3-(4-fluorophenyl)-3-(4-hydroxyphenyl)-acrylate
https://huagongshe.com/reaction/731168
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl trimethylsilylacetate | HCID 77687 | — |
| Edukt | 4-Fluoro-4'-hydroxybenzophenone | HCID 117666 | — |
| Edukt | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethyl 3-(4-fluorophenyl)-3-(4-hydroxyphenyl)-acrylate | HCID 68674988 | — |
Reaktionsschritte
A solution of lithium hexamethyldisilazide (23.1 mL, 1 M in THF) was added to a stirred solution of ethyl (trimethylsilyl)acetate (2.53 mL, 13.9 mmol) in THF (15 mL) in 10 minutes at −78° C. The reaction mixture was further stirred at this temperature for 20 minutes. A solution of (4-fluoro-phenyl)-(4-hydroxy-phenyl)-methanone (2 g, 9.2 mmol) in THF (30 mL) was slowly added to the reaction mixture. The reaction mixture was brought to 0° C. over 5 hours. The reaction mixture was quenched with saturated ammonium chloride solution, extracted into EtOAc and washed with dilute ammonium chloride solution. The organic layer was dried over magnesium sulfate. The solvent was removed under vacuum, and the resulting product was flash chromatographed on silica gel, giving M1.1 as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07582803B2 |
|---|
| Quelldatensatz | uspto-grants-2009_09 |
|---|
| ORD ID | ord-c3b17590bdc5410d85a69b887de178d7 |
|---|
| Quellennotiz | uspto-grants-2009_09 |
|---|