HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Sulfate → N-ethyl phenazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Sulfate | HCID 6163 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethoxyethane;phenazine | HCID 67351390 | — |
| Product | N-ethyl phenazine | HCID 15309770 | — |
Reaction Steps
Scheme 6 illustrates the synthesis of N-ethyl phenazine 1-hydroxybutyl methyl ether. The phenazine ether (21) is prepared by the alkylation of the 1-hydroxyphenazine (1) with 4-methoxybutylbromide (Aldrich Chemical Company, USA) to give phenazine derivative (21). N-ethyl phenazine (22) is prepared by reaction of compound (21) with diethyl sulfate in the presence of potassium carbonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08008037B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-b919a525f7ca43aeb1fa60aeb1993002 |
| Source note | uspto-grants-2011_08 |