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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21475Generated: October 26, 2026

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

https://huagongshe.com/reaction/21475

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzeneHCID 19374470—
CatalystHCID 178418390HCID 178418390—
SolventTolueneHCID 1140—
Product4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamineHCID 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 atms. 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424277
Source datasetuspto-grants-1995_06
ORD IDord-67f78207c5b64f1ab0a8cb7a7aad0bee
Source noteuspto-grants-1995_06