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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262012Generated: October 25, 2026

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

https://huagongshe.com/reaction/262012

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 hrs., 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 numberUS04153446
Source datasetuspto-grants-1979_05
ORD IDord-9cc3f965c1b640e1b7d43fc85411ead5
Source noteuspto-grants-1979_05