Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963766Generated: October 31, 2026

2-Fluoro-4-nitrophenol → HCID 68748084, compound

https://huagongshe.com/reaction/1963766

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-4-nitrophenolHCID 9825—
ReactantPotassium CarbonateHCID 11430—
ReactantHomoallyl bromideHCID 21241—
SolventAcetonitrileHCID 6342—
ProductHCID 68748084HCID 68748084—

Reaction Steps

To an acetonitrile (40 mL) solution of 2-fluoro-4-nitrophenol (2.36 g; 15.1 mmol) and potassium carbonate (2.77 g; 20.1 mmol), 4-bromo-1-butene (2.81 g; 20.4 mmol) was added, and the mixture was refluxed and then reacted for 16 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)-3-fluoronitrobenzene (1d) (2.57 g, 81% 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-e78102feb87d4a42830a5b44c4393dfb
Source noteuspto-grants-2013_04