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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684319Generated: November 3, 2026

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

https://huagongshe.com/reaction/1684319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBromocyclopentaneHCID 8728—
ReactantSodium HydroxideHCID 14798—
ReactantBis(2-chloro-4-fluoro-5-aminophenyl)carbonateHCID 15766649—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Product4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamineHCID 15279389192.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A round-bottomed flask (50 cc) was charged with bis(5-amino-2-chloro-4-fluorophenyl)carbonate (1.52 g, 4.36 mmol), cyclopentyl bromide (1.39 g, 9.29 mmol) and tetrabutylammonium bromide (74 mg, 0.23 mmol) to prepare a solution in toluene (12 mL). Subsequently, 48% sodium hydroxide in aqueous solution (6 mL) was added slowly and the mixture was stirred under heating at 80° C. for 1 h. After completion of the reaction, the reaction mixture was cooled to room temperature and water (15 mL) was added, followed by extraction with toluene (10 mL×2). The organic layers were combined and washed with water (10 mL×2). The solvent was distilled off under vacuum from the resulting toluene solution, thereby giving 4-chloro-5-cyclopentyloxy-2-fluoroaniline (1.93 g, 8.40 mmol; yield=96.3% ).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639915
Source datasetuspto-grants-1997_06
ORD IDord-bfda8d0e14dd4499b2c50ac12f9c4c6e
Source noteuspto-grants-1997_06