HuagongsheHuagongshe Chemistry Print Report · For research reference only
1h-Indazole,4-(2-fluoro-4-nitrophenoxy)- → 3-Fluoro-4-(1H-indazol-4-yloxy)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1h-Indazole,4-(2-fluoro-4-nitrophenoxy)- | HCID 17979311 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Product | 3-Fluoro-4-(1H-indazol-4-yloxy)aniline | HCID 17979339 | — |
Reaction Steps
Under argon, 60 mg (0.22 mmol) of 4-(2-fluoro-4-nitrophenoxy)-1H-indazole (from example XXV) are initially charged in 5 ml of ethanol/tetrahydrofuran (1:1), 9.97 mg (0.04 mmol) of platinum(IV) oxide are added and the mixture is hydrogenated under atmospheric pressure for 2 hours. The suspension is filtered off through CELITE (diatomaceous earth), the filtercake is washed with ethanol and the filtrate is concentrated under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737153B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-d48c9432d27d412c9e71f902df366c04 |
| Source note | uspto-grants-2010_06 |