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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 128544Erstellt: 25. Oktober 2026

2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzene → 4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamine

https://huagongshe.com/reaction/128544

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzeneHCID 19374470—
KatalysatorHCID 178418390HCID 178418390—
LösungsmittelTolueneHCID 1140—
Produkt4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamineHCID 15279389—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05464811
Quelldatensatzuspto-grants-1995_11
ORD IDord-7515f32f23354524b33cb983359adfa9
Quellennotizuspto-grants-1995_11