HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Propionate ion → 3-(2-Nitrophenyl)isoxazolin-5-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Propionate ion | HCID 104745 | — |
| Edukt | Butyrate | HCID 104775 | — |
| Edukt | Hydroxyamine hydrochloride | HCID 443297 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Edukt | Ethyl 2-nitro-beta-oxobenzenepropanoate | HCID 10561837 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 3-(2-Nitrophenyl)isoxazolin-5-one | HCID 21271853 | — |
Reaktionsschritte
The reactions of Equations 15a and 15b above can be run by procedures similar to those described in U.S. Pat. No. 3,781,438 for the preparation of 5-halo-3-phenylisoxazoles. Thus, in reaction 15a, an ethyl 2-(2-nitrobenzoyl)acetate, propionate or butyrate of Formula (XIV) is reacted with hydroxylamine hydrochloride and sodium acetate in ethanol at reflux for 0.5 to 5 hours to form a 3-(2-nitrophenyl)isoxazolin-5-one of Formula (XXVI). In reaction 15b, XXVI is reacted with an equimolar amount of triethylamine and excess phosphorus oxychloride or phosphorus oxybromide in toluene at 25° to 110° C. for 1 to 5 hours to form Xc"'.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04606755 |
| Quelldatensatz | uspto-grants-1986_08 |
| ORD ID | ord-cb8e304acedb42a3ba4e8998b434a0dc |
| Quellennotiz | uspto-grants-1986_08 |