HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrobenzene → Azoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | 1-Ethyl-2-nitrobenzene | HCID 69156 | — |
| Product | Azoxybenzene | HCID 10316 | — |
Reaction Steps
The reduction reaction was carried out in the same manner as set forth in Example 6 except for using a mixture of 1.0 mmol of nitrobenzene and 1.0 mmol of o-ethyl nitrobenzene instead of using nitrobenzene alone, and using 16.5 mg (the amount required for swelling of the reactant, i.e., the mixture, in 100%) of Polymer supported reagent-2, and thereby an azoxybenzene derivative of a symmetrical structure and an azoxybenzene derivative of an asymmetrical structure were obtained as a main product, respectively. Besides, a small amount of an azobenzene derivative of a symmetrical structure was also synthesized.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09169200B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-d3f8db800dfd4995a1e7b85d928abddc |
| Source note | uspto-grants-2015_10 |