HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5549Erstellt: 24. Oktober 2026
Hydrochloric Acid → 1,5-Di(2-furyl)-3-(2,4-dimethoxyphenyl)-1,5-pentanedione
https://huagongshe.com/de/reaction/5549
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 2-Acetylfuran | HCID 14505 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 2,4-Dimethoxybenzaldehyde | HCID 69175 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1,5-Di(2-furyl)-3-(2,4-dimethoxyphenyl)-1,5-pentanedione | HCID 15001912 | — |
Reaktionsschritte
Following the general methods outlined by Weller and Luellen (see above), to a solution of 16.6 g (0.1 mole) of 2,4-dimethoxybenzaldehyde 1 and 20 ml (0.2 mole) of 2-acetylfuran 2 in 100 ml of methanol was added 5.5 g of potassium hydroxide previously dissolved in a small amount of methanol. The resulting mixture was heated to reflux and then stirred overnight at 55° C. The solution was then poured into water acidified with 1N HCl and extracted with CH2Cl2. The CH2Cl2 extracts were dried (Na2SO4) and the solvents removed at high vacuum. The resulting amber oil solidified on standing overnight affording 36.7 g of crude dione 3.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05245038 |
|---|
| Quelldatensatz | uspto-grants-1993_09 |
|---|
| ORD ID | ord-a5d5033460474ef09b7089853a326df4 |
|---|
| Quellennotiz | uspto-grants-1993_09 |
|---|