HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 359356Erstellt: 25. Oktober 2026
3,4,5-Trimethoxybenzaldehyde → 2,2-Dimethyl-5-[2-(3,4,5-trimethoxyphenyl)ethenyl]-3(2H)-furanone
https://huagongshe.com/reaction/359356
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3,4,5-Trimethoxybenzaldehyde | HCID 6858 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 3(2H)-Furanone, 2,2,5-trimethyl- | HCID 137080 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2,2-Dimethyl-5-[2-(3,4,5-trimethoxyphenyl)ethenyl]-3(2H)-furanone | HCID 53716106 | 83% |
Reaktionsschritte
To a mixture of 2,2,5-trimethyl-3(2H)-furanone (2.5 g, 19.8 mM) and 3,4,5-trimethoxybenzaldehyde (4.7 g, 23.8 mM) in ethanol was added 1N aqueous sodium hydroxide (4 mL, 4mM). After the reaction mixture was stirred for 48 hours at room temperature, the solution was concentrated to 50 mL and diluted with water (300 mL). The aqueous layer was extracted with diethyl ether (4×100 mL). The combined ethereal extracts were washed with saturated aqueous sodium chloride (50 mL), dried over magnesium sulfate, filtered and concentrated under reduced pressure to afford a dark yellow crystalline solid. The crude product was purified by chromatography (silica gel, petroleum ether-ethyl acetate) to give light yellow crystals (5.0 g, 83% yield), m.p. 149°-150° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05001126 |
|---|
| Quelldatensatz | uspto-grants-1991_03 |
|---|
| ORD ID | ord-35d8c43986d044b590463d0e55aa15d7 |
|---|
| Quellennotiz | uspto-grants-1991_03 |
|---|