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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963756Generated: October 25, 2026

4-Nitrophenol → 4-(3-Butenyloxy)nitrobenzene

https://huagongshe.com/reaction/1963756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantPotassium CarbonateHCID 11430—
ReactantHomoallyl bromideHCID 21241—
SolventAcetonitrileHCID 6342—
Product4-(3-Butenyloxy)nitrobenzeneHCID 11217769—

Reaction Steps

To an acetonitrile (20 mL) solution of 4-nitrophenol (0.423 g; 3.04 mmol) and potassium carbonate (1.11 g; 8.02 mmol), 4-bromo-1-butene (0.827 g; 6.13 mmol) was added, and the mixture was refluxed and then reacted for 17 hours. After completion of the reaction, the solution was filtrated by Celite, and then the filtrate was concentrated under a reduced pressure. The residue was purified by flash column chromatography using methylene chloride, and then the effluent was concentrated to obtain 4-(3-butenyloxy)nitrobenzene (1) (0.571 g, 97% of yield, a light yellow oil) represented by the following formula.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415451B2
Source datasetuspto-grants-2013_04
ORD IDord-8e893467d62f41b6a57c287f23c04925
Source noteuspto-grants-2013_04