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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855702Generated: October 31, 2026

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

https://huagongshe.com/reaction/1855702

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 numberUS04216152
Source datasetuspto-grants-1980_08
ORD IDord-b12259e8c372437c99957bc9d712d514
Source noteuspto-grants-1980_08