HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Nitrobenzaldehyde → 5-(4-Nitrophenyl)-1,3-oxazole
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Nitrobenzaldehyde | HCID 541 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Tosylmethyl isocyanide | HCID 161915 | — |
| Katalysator | Tetrabutylammonium Bromide | HCID 74236 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-(4-Nitrophenyl)-1,3-oxazole | HCID 2737068 | 144,8% |
Reaktionsschritte
To an aqueous solution containing 0.84 g of sodium hydroxide were added 0.45 g of 4-nitrobenzaldehyde, 12.2 g of a methylene chloride solution containing 0.65 g of TosMIC which was obtained in the same way as that of Example 6 and 0.10 g of tetrabutyl ammonium bromide at room temperature. The mixture was allowed to react at room temperature until HPLC found no trace of the starting materials. Upon the completion of the reaction, the reaction solution was washed with water and dried over anhydrous magnesium sulfate. The solvents were distilled off. An HPLC analysis showed that the concentrated residue contained 0.82 g of the target compound (yield: 93%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | USRE040795E1 |
| Quelldatensatz | uspto-grants-2009_06 |
| ORD ID | ord-3650e42fe4904bae8e7195da84648b4e |
| Quellennotiz | uspto-grants-2009_06 |