HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 322257Erstellt: 25. Oktober 2026
1,3-Dichloroacetone → 4-Chloromethyl-2-styryl-oxazole
https://huagongshe.com/reaction/322257
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,3-Dichloroacetone | HCID 10793 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2-Propenamide, 3-phenyl- | HCID 12135 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-Chloromethyl-2-styryl-oxazole | HCID 22009752 | 47% |
Reaktionsschritte
A mixture of cinnamamide (25.3 g) and 1,3-dichloroacetone (20.9 g) was stirred for one hour at 130° C. The reaction mixture was diluted with water, neutralized with potassium carbonate, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4), and concentrated under reduced pressure. The residue was subjected to a silica gel column chromatography. From the fraction eluted with diethyl ether-hexane, 4-chloromethyl-2-[(E)-2-phenylethenyl]oxazole (16.9 g, 47%) was obtained. Recrystallization from diethyl ether-hexane gave colorless needles, mp 72-73° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06211215B1 |
|---|
| Quelldatensatz | uspto-grants-2001_04 |
|---|
| ORD ID | ord-60507feac8c145038b96233133a1f837 |
|---|
| Quellennotiz | uspto-grants-2001_04 |
|---|