Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128544Generated: October 26, 2026

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

https://huagongshe.com/reaction/128544

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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464811
Source datasetuspto-grants-1995_11
ORD IDord-7515f32f23354524b33cb983359adfa9
Source noteuspto-grants-1995_11