Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861277Generated: October 30, 2026

5-Fluoro-2-nitrophenol → HCID 86747314, compound

https://huagongshe.com/reaction/861277

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-2-nitrophenolHCID 9937—
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantHomoallyl bromideHCID 21241—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 86747314HCID 86747314—

Reaction Steps

To a suspension of NMP (20 ml), acetone (20 ml) and potassium carbonate (8.85 ) was added 5-fluoro-2-nitro phenol (5.0 g, 30 mmol) in one portion. After 15 minutes, the suspension began to turn yellow. After stirring 30 minutes under nitrogen, 4-bromobutene (4.25 ml) was added and the suspension was refluxed for 18 hours. The suspension was poured into water and extracted with 3×200 ml of diethyl ether. The aqueous layer was acidified with 2N HCl and extracted with ether. The ether layers were combined, washed with 2N HCl and water and dried over anhydrous magnesium sulfate. Filtration and in vacuo concentration yielded 6.0 g of 2-(3-butenyloxy-4-fluoronitrobenzene, as an oil, which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05714304
Source datasetuspto-grants-1998_02
ORD IDord-0d372059de2c4276903a69fe8f1555a2
Source noteuspto-grants-1998_02