HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Aniline → Formanilide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Aniline | HCID 6115 | — |
| Edukt | Carbanilide | HCID 7595 | — |
| Edukt | Formanilide | HCID 7671 | — |
| Katalysator | Ruthenium | HCID 23950 | — |
| Produkt | Formanilide | HCID 7671 | — |
| Produkt | p-Toluidine | HCID 7813 | — |
| Produkt | 1-(4-Methylphenyl)-3-phenylurea | HCID 572170 | — |
Reaktionsschritte
Watanabe et al. (J. Chem. Soc., Chem. Commun. (1990) 1497) reported a synthesis of N,N'-diphenylurea in 92% yield by dehydrogenating formanilide in the presence of aniline and a ruthenium catalyst: ##STR2## Watanabe et al. prepared numerous symmetric N,N'-diarylureas in this manner. In contrast, N-phenyl-N'-p-tolylurea was not obtained selectively from the reaction of formanilide and p-toluidine. Instead, a mixture of three ureas -- N,N'-diphenylurea (19%), N,N'-di-p-tolylurea (21%), and the unsymmetric product, N-phenyl-N'-p-tolylurea (38%) -- was obtained:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05155267 |
| Quelldatensatz | uspto-grants-1992_10 |
| ORD ID | ord-3f4e9027ed884b30bddbbede4b6e84d6 |
| Quellennotiz | uspto-grants-1992_10 |