HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → Diallylglycidylurazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Perpropionic acid | HCID 65136 | — |
| Reactant | Trisallylurazole | HCID 20253124 | — |
| Product | Diallylglycidylurazole | HCID 20253115 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04562274 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-0a2156b74f054fd0b919e929ccd536e7 |
| Source note | uspto-grants-1985_12 |