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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250829Generated: November 1, 2026

p-Fluoronitrobenzene → 2,6-Ditert-butyl-4-(4-nitrophenyl)phenol

https://huagongshe.com/reaction/2250829

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-Di-tert-butylphenolHCID 31405—
SolventDimethyl SulfoxideHCID 679—
Product2,6-Ditert-butyl-4-(4-nitrophenyl)phenolHCID 1734905—

Reaction Steps

8.40 g (40.7 mmol) 2,6-di-tert-butylphenol was dissolved in 100 ml dried DMSO. 8 g (58 mmol) potassium carbonate and 7.6 g (54 mmol) p-fluoronitrobenzene were added into the DMSO solution. The DMSO solution was heated to 100˜120° C. for 12 hrs with stirring. Then the reaction mixture was allowed to cool to room temperature and poured into distilled water. The aqueous solution was acidified to pH 2˜4 and yellow precipitate was collected by filtration. The yellow precipitate was washed with water and dried. The crude yield was 75%. The yellow precipitate was purified by recrystallizing in cyanomethane, mp 157˜160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317110B2
Source datasetuspto-grants-2008_01
ORD IDord-63242472b8d54ccd9230861bfa7c5199
Source noteuspto-grants-2008_01