HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethyl formate → Formamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethyl formate | HCID 8025 | — |
| Edukt | Methyl 3-carbamoylisobutyrate | HCID 11768702 | — |
| Produkt | Formamide | HCID 713 | — |
| Produkt | Methylsuccinic acid ethyl methyl ester | HCID 54001611 | — |
Reaktionsschritte
The procedure in Example 3 (3) was repeated except that ethyl formate was used in place of methyl formate. As a result, the conversion of methyl 3-carbamoylisobutyrate was 83.7% and there were obtained methylsuccinic acid ethyl methyl ester at a selectivity of 99.8% and formamide at a selectivity of 98.6%, each based on the reacted methyl 3-carbamoylisobutyrate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05618953 |
| Quelldatensatz | uspto-grants-1997_04 |
| ORD ID | ord-0b2414389f2d435ebd782a575159d2a6 |
| Quellennotiz | uspto-grants-1997_04 |