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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770127Generated: November 1, 2026

4-tert-Butylphenol → HCID 15225594, compound

https://huagongshe.com/reaction/1770127

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylphenolHCID 7393—
ReactantPotassium CarbonateHCID 11430—
Reactant3-BromobenzonitrileHCID 23381—
ReactantPotassium bisulfateHCID 516920—
SolventPyridineHCID 1049—
ProductHCID 15225594HCID 1522559454%

Reaction Steps

To a solution of 3-bromobenzonitrile (4.35 g, 23.9 mmol) and p-t-butylphenol (4.30 g, 28.7 mmol) in pyridine (45 ml) were added potassium carbonate (6.61 g, 47.8 mmol) and cupric oxide (3.42 g, 43 mmol), and the resultant mixture was refluxed for 46 hours. The reaction mixture was poured into saturated potassium hydrogensulfate solution and extracted with ethyl acetate. The organic layer was concentrated, and the residue was dissolved in ethylene glycol (20 ml), mixed with 2N potassium hydroxide solution (130 ml) and refluxed for 20 hours. The reaction mixture was poured into chilled water and extracted with diethyl ether under acidic conditions. The organic layer was dried and concentrated. The residue was chromatographed on a silica gel column to give the titled compound (3.46 g, yield 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05385917
Source datasetuspto-grants-1995_01
ORD IDord-1222ec5818264b4799c8833871b84b14
Source noteuspto-grants-1995_01