HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
N-(2-Furoyl)Glycine → (4Z)-2-(2-furyl)-4-[(5-phenyl-2-furyl)methylene]-1,3-oxazol-5(4H)-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | N-(2-Furoyl)Glycine | HCID 21863 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Edukt | 5-Phenyl-2-furaldehyde | HCID 2769420 | — |
| Lösungsmittel | Acetic Anhydride | HCID 7918 | — |
| Produkt | (4Z)-2-(2-furyl)-4-[(5-phenyl-2-furyl)methylene]-1,3-oxazol-5(4H)-one | HCID 22148173 | 33,3% |
Reaktionsbedingungen
| Temperatur | 60 °C |
|---|
Reaktionsschritte
As illustrated in Scheme 2, N-2-furoylglycine (131 mg, 0.776 mmol) is suspended in acetic anhydride (1 mL) and sodium acetate (76 mg, 0.931 mmol) and 5-phenylfuraldehyde (170 mg, 1 mmol) are added. The reaction mixture is shaken at 60° C. for one hour, and cooled to 0° C. The resulting orange solid is filtered and washed with ice water (75 mL) and heptane (50 mL). The solid is then dried under vacuum at 40° C. to afford 79 mg of (4Z)-2-(2-furyl)-4-[(5-phenyl-2-furyl)methylene]-1,3-oxazol-5(4H)-one which was used without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07041690B2 |
| Quelldatensatz | uspto-grants-2006_05 |
| ORD ID | ord-c1baa3e6c33147469c37db0a4ec3b651 |
| Quellennotiz | uspto-grants-2006_05 |