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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720428Generated: October 30, 2026

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

https://huagongshe.com/reaction/1720428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
Reactantmethyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamateHCID 15766845—
SolventWaterHCID 962—
Product4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamineHCID 1527938998.3%

Reaction Steps

A 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), followed by refluxing under heating for 5 hours. After completion of the reaction, the reaction solution was cooled to room temperature, water (5 liters) was added thereto, and the mixture was extracted with toluene (5 liters×2 portions). The organic layer was washed with water and dried over anhydrous magnesium sulfate. The drying agent was separated by filtration, and the filtrate was distilled off under reduced pressure to obtain 2-fluoro-4-chloro-5-cyclopentyloxyaniline as an oily substance (1.75 Kg, 7.62 mol, 98.3% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506190
Source datasetuspto-grants-1996_04
ORD IDord-9303ea6f76ae414492fb0f6becff9ab9
Source noteuspto-grants-1996_04