HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 3,6-di(p-nitrostyryl)pyridazine-N-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 3,6-Di(p-nitrostyryl)pyridazine | HCID 54059565 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 3,6-di(p-nitrostyryl)pyridazine-N-oxide | HCID 53898164 | — |
Reaction Steps
33 g of this nitro compound (K') is reacted, with 15g of m-chloroperbenzoic acid in halogen-containing solvent (such as 1,2-dichloroethane) to obtain 27 g of 3,6-di(p-nitrostyryl)pyridazine-N-oxide (L'). The nitro group in the N-oxide compound (L') is selectively reduced under a neutral or basic condition to obtain 20 g of vermilion crystals of 3,6-di(p-aminostyryl)pyridazine-N-oxide (M').
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04871633 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-68aa9fcf577c46728686b02ffd3854ff |
| Source note | uspto-grants-1989_10 |