HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzene → 4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzene | HCID 19374470 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamine | HCID 15279389 | — |
Reaction Steps
The resulting 2-fluoro-4-chloro-5-cyclopentyloxynitrobenzene (13.0 g, 50.1 mmol) was dissolved in toluene (100 ml), a catalytic amount of 10% palladium-carbon (0.5 g) was added thereto, and the mixture was reacted at room temperature to 70° C. under a hydrogen pressure of 3 to 5 arms. in a glass autoclave. After absorption of hydrogen gas ceased, the catalyst was removed by filtration, and the solvent was distilled off under reduced pressure from the filtrate to obtain substantially quantitatively oily 2-fluoro-4-chloro-5-cyclopentyloxyaniline. The spectral data and the like are as described in Reference Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05464811 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-7515f32f23354524b33cb983359adfa9 |
| Source note | uspto-grants-1995_11 |