HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Nitrophenol → HCID 178476832, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Nitrophenol | HCID 980 | — |
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Benzyl chloroformate | HCID 10387 | — |
| Edukt | Phosphorus pentachloride | HCID 24819 | — |
| Edukt | Diethyl p-aminobenzylphosphonate | HCID 88358 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Sodium Bicarbonate | HCID 516892 | — |
| Produkt | HCID 178476832 | HCID 178476832 | — |
Reaktionsschritte
Diethyl p-aminobenzylphosphonate (1) (Aldrich Chemical Co., Milwaukee, WI) was converted to the p-carbobenzyloxy derivative (2) by the addition of 1.2 equivalents benzyl chloroformate in saturated aqueous sodium bicarbonate (NaHCO3) for 20 minutes at 23° C. That derivative was treated with 1.1 equivalents phosphorous pentachloride (PCl5) in chloroform at 50° C. for 2 hours. Pyridine (5 equivalents) and p-nitrophenol (3 equivalents) were added at 23° C. and subsequent workup provided the ethyl p-nitrophenyl phosphonate (3).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04659567 |
| Quelldatensatz | uspto-grants-1987_04 |
| ORD ID | ord-557e42d8b708457abe6792d4987dd115 |
| Quellennotiz | uspto-grants-1987_04 |