HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzene → Diallylglycidylurazole
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzene | HCID 241 | — |
| Edukt | Perpropionic acid | HCID 65136 | — |
| Edukt | Trisallylurazole | HCID 20253124 | — |
| Produkt | Diallylglycidylurazole | HCID 20253115 | — |
Reaktionsschritte
6.895 kg (35 mol) of trisallylurazole were reacted with 31.5 kg of a 22% strength solution of perpropionic acid in benzene (77 mol) at 60° C. in a manner analogous to that described in Example 1. After a reaction time of 10 hours, the percarboxylic acid conversion was 97.2% and the conversion of trisallylurazole was 94.6%. Diallylglycidylurazole was formed in a selectivity of 28.3%, allyldiglycidylurazole was formed in a selectivity of 41.2% and trisglycidylurazole was formed with a selectivity of 20.1%, in each case based on the trisallylurazole reacted.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04562274 |
| Quelldatensatz | uspto-grants-1985_12 |
| ORD ID | ord-0a2156b74f054fd0b919e929ccd536e7 |
| Quellennotiz | uspto-grants-1985_12 |