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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395354Generated: November 3, 2026

2-Nitrophenol → 1-(Cyclopentyloxy)-2-nitrobenzene

https://huagongshe.com/reaction/1395354

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrophenolHCID 6947—
ReactantBromocyclopentaneHCID 8728—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
Product1-(Cyclopentyloxy)-2-nitrobenzeneHCID 2216447346.8%

Reaction Steps

2-Nitrophenol (83.5 g, 0.60 mole), cyclopentyl bromide (98.0 g, 0.66 mole), anhydrous potassium carbonate (82.9 g, 0.60 mole) and dry acetone (600 cc) were refluxed for 72 hours, and filtered to remove the potassium bromide. The residue was washed with acetone and the solvent was removed by rotary evaporation. The residue was partitioned between 200 cc of dichloromethane and water. The dichloromethane layer was washed with 200 cc of 10% potassium hydroxide, separated and the solvent was removed by rotary evaporation. The crude product was fractionally distilled at 144°-146° C. at 1.0 mm. Hg to yield 58.2 g of product (46.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04203901
Source datasetuspto-grants-1980_05
ORD IDord-58a327a77b474e7b9dd77fb50849ffe3
Source noteuspto-grants-1980_05