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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128543Generated: October 26, 2026

Potassium Carbonate → 2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzene

https://huagongshe.com/reaction/128543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenol, 2-chloro-4-fluoro-5-nitro-HCID 158655—
ReactantCyclopentyl 4-methylbenzene-1-sulfonateHCID 317685—
SolventAcetonitrileHCID 6342—
Product2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzeneHCID 1937447092.6%

Reaction Steps

A solution of 2-fluoro-4-chloro-5-hydroxynitrobenzene (7.1 g, 37.1 mmol) and potassium carbonate (5.1 g, 37.1 mmol) in acetonitrile (300 ml) was stirred for 2 hours at a refluxing temperature. Cyclopentyl p-toluenesulfonate (10.3 g, 40.8 mmol) was added thereto, followed by stirring further for 2 hours under refluxing. After completion of the reaction, the solvent was distilled off under reduced pressure from the reaction mixture, 1N hydrochloric acid (800 ml) was added thereto, and the mixture was extracted with ethyl acetate (100 ml×3 times). The organic layer was washed with an aqueous solution of sodium bicarbonate and water, dried, and the solvent was distilled off under reduced pressure to obtain 2-fluoro-4-chloro-5-cyclopentyloxynitrobenzene as a yellow solid (8.93 g, 34.3 mmol, 92.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464811
Source datasetuspto-grants-1995_11
ORD IDord-e6cee3e6b5ac4c1d9fc5123fc3052065
Source noteuspto-grants-1995_11