HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1193210Erstellt: 25. Oktober 2026
2,2,5,5-Tetramethyltetrahydro-3-ketofuran → 4-(5-Bromo-2-ethylbenzylidene)-2,2,5,5-tetramethyldihydrofuran-3-one
https://huagongshe.com/reaction/1193210
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2,2,5,5-Tetramethyltetrahydro-3-ketofuran | HCID 138511 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | 5-Bromo-2-ethylbenzaldehyde | HCID 54772389 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | 1,2-Dimethoxyethane | HCID 8071 | — |
| Produkt | 4-(5-Bromo-2-ethylbenzylidene)-2,2,5,5-tetramethyldihydrofuran-3-one | HCID 66823198 | 94,9% |
Reaktionsschritte
To an ice-cold solution of dihydro-2,2,5,5-tetramethyl-3(2H)-furanone (13.4 g, 94.34 mmol) in anhydrous 1,2-dimethoxyethane (32 ml) is added sodium methoxide (5.6 g, 103.8 mmol) in one portion, and the reaction mixture is stirred at this temperature for 5 minutes. To the resulting slurry is then added a solution of 5-bromo-2-ethyl-benzaldehyde (20 g, 94.34 mmol) in 1,2-dimethoxyethane (32 ml) dropwise over 10 minutes. The solution is next stirred at 0° C. for 1 hour, then diluted with diethyl ether and washed with 2M hydrochloric acid (×2). Organic fractions are combined, dried over magnesium sulphate, filtered and the filtrate evaporated in vacuo to afford 4-(5-bromo-2-ethylbenzylidene)-2,2,5,5-tetramethyldihydrofuran-3-one (30.2 g) as a yellow liquid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08680299B2 |
|---|
| Quelldatensatz | uspto-grants-2014_03 |
|---|
| ORD ID | ord-7bc896f77bd045c0b0bd530e8011a2b7 |
|---|
| Quellennotiz | uspto-grants-2014_03 |
|---|