HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-4-nitrobenzene → 4-{[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-4-nitrobenzene | HCID 11466 | — |
| Reactant | 4-(4-Nitrophenoxy)benzenamine | HCID 80251 | — |
| Reactant | 2,3-Dichloro-5-(trifluoromethyl)pyridine | HCID 112234 | — |
| Product | 4-{[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}aniline | HCID 2764116 | — |
Reaction Steps
In the above (B), 4-bromonitrobenzene was replaced with 2,3-dichloro-5-trifluoromethylpyridine to obtain 4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)aniline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04976773 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-044ea9d4cffc4018b7d8e6feb5f14f9c |
| Source note | uspto-grants-1990_12 |