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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963762Generated: October 31, 2026

2-Methyl-4-nitrophenol → HCID 68752044, compound

https://huagongshe.com/reaction/1963762

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-4-nitrophenolHCID 7442—
ReactantPotassium CarbonateHCID 11430—
ReactantHomoallyl bromideHCID 21241—
SolventAcetonitrileHCID 6342—
ProductHCID 68752044HCID 68752044—

Reaction Steps

To an acetonitrile (50 mL) solution of 2-methyl-4-nitrophenol (3.05 g; 19.9 mmol) and potassium carbonate (4.27 g; 30.9 mmol), 4-bromo-1-butene (4.02 g; 29.8 mmol) was added, and the mixture was refluxed and then reacted for 12 hours. After completion of the reaction, the solution was filtrated by Celite, and then 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)-2-methylnitrobenzene (1c) (2.61 g, 63% 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-9f221d2e4a7c441c862d2f3fd5e98277
Source noteuspto-grants-2013_04