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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275099Erstellt: 25. Oktober 2026

Ethanol → 4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamine

https://huagongshe.com/reaction/275099

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktPotassium HydroxideHCID 14797—
Eduktmethyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamateHCID 15766845—
LösungsmittelWaterHCID 962—
Produkt4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamineHCID 1527938998,3%

Reaktionsschritte

4N potassium hydroxide aqueous solution (4.75 liters) was added to an ethanol solution (3 liters) of methyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate (2.25 kg, 7.85 mol) and the mixture was heated under reflux for 5 hours. After reaction, the reaction liquid was cooled to room temperature, water (5 liters) was added thereto, and this was extracted with toluene (5 liters×2). The organic layer was washed with water and then dried over anhydrous magnesium sulfate. The drying agent was taken out by filtration, and the solvent was removed by distillation under reduced pressure to obtain an oily product of 2-fluoro-4-chloro-5-cyclopentyloxyaniline (1.75 kg, 7.62 mol). Yield: 98.3%. Spectral data and other data of the product are those as shown in Example 21.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05391807
Quelldatensatzuspto-grants-1995_02
ORD IDord-26a7ca6f0d9d415bb97985d3cdfe3487
Quellennotizuspto-grants-1995_02