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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21474Generated: October 26, 2026

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

https://huagongshe.com/reaction/21474

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, in hydrochloric acid (300 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 numberUS05424277
Source datasetuspto-grants-1995_06
ORD IDord-0b1ea39f652a4ec0b1ad722b5587f73d
Source noteuspto-grants-1995_06