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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230997Generated: October 31, 2026

Bromocyclopentane → 1-Cyclopentyloxy-2-methoxy-5-nitrobenzene

https://huagongshe.com/reaction/2230997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromocyclopentaneHCID 8728—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methoxy-5-nitrophenolHCID 69471—
ReactantSodium BicarbonateHCID 516892—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-Cyclopentyloxy-2-methoxy-5-nitrobenzeneHCID 11390741—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2-methoxy-5-nitrophenol (4.86 g), cyclopentyl bromide (3.4 ml) and potassium carbonate (4.8 g) in N,N-dimethylformamide (50 ml) was stirred at 50° C. for 3 hours. Then the mixture was poured into a mixture of ethyl acetate and aqueous sodium bicarbonate. The organic phase was separated, washed with aqueous sodium bicarbonate and brine, dried over magnesium sulfate and concentrated. The resultant solid was collected and washed with isopropyl ether to give 3-cyclopentyloxy-4-methoxy-1-nitrobenzene (5.05 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426345B1
Source datasetuspto-grants-2002_07
ORD IDord-a2333078922e441096099ec0aa511ca9
Source noteuspto-grants-2002_07