HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Chloro-5-fluoro-4-(quinolin-3-yloxy)phenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Chloro-5-fluoro-4-(quinolin-3-yloxy)nitrobenzene | HCID 22148734 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Chloro-5-fluoro-4-(quinolin-3-yloxy)phenylamine | HCID 22148812 | 47.3% |
Reaction Steps
To a solution of 3-chloro-5-fluoro-4-(quinolin-3-yloxy)nitrobenzene (50.1) (0.980 g) and NH4Cl (1.64 g) in EtOH(50 mL)—H2O (5 mL), was added iron powder (1.92 g). The mixture was heated to reflux for 1 h. After cooling the reaction mixture was filtered through short celite pad. The filtrate was concentrated, diluted with sat.NaHCO3 and extracted with AcOEt (30 mL×3). The combined organic layers were washed with brine and dried over Na2SO4. Concentration of solvent afford crude product, which was purified by column chromatography (silica gel, AcOEt:hexane=1:3) to provide aniline 50.2 (0.420 g) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06583157B2 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-b91882584b0646b89e1b79c8b8bf1b84 |
| Source note | uspto-grants-2003_06 |