HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-phenyl-m-anisidine → 4-Methoxy-10H-phenothiazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-phenyl-m-anisidine | HCID 7544 | — |
| Reactant | Methyl phenothiazin-2-yl ether | HCID 74490 | — |
| Product | 4-Methoxy-10H-phenothiazine | HCID 19828346 | — |
Reaction Steps
The conversion rate of the 3-methoxydiphenylamine is 91%, and the chemical yield of 2-methoxyphenothiazine is 91%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05026846 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-9d28eb95d5ea47f6934f3116e70fe92f |
| Source note | uspto-grants-1991_06 |