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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576667Generated: November 1, 2026

Ethyl Acetate → 4-(4-Bromo-3,5-dimethylphenoxy)-2-methylbutan-2-ol

https://huagongshe.com/reaction/576667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-3,5-dimethylphenolHCID 81970—
Reactant2-Methyl-4-[(4-methylbenzenesulfonyl)oxy]butan-2-olHCID 14001295—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(4-Bromo-3,5-dimethylphenoxy)-2-methylbutan-2-olHCID 6797292191%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixed solution of 3-hydroxy-3-methylbutyl 4-methylbenzenesulfonate (4.24 g) synthesized in accordance with the method described in [WO 2009/067613 pamphlet, Example 308], 4-bromo-3,5-dimethylphenol (3.0 g), and potassium carbonate (3.09 g) in N,N-dimethylformamide (15 mL) was stirred at 80° C. for 3 hours. To the reaction mixture, ethyl acetate (200 mL) and water (100 mL) were added and the mixture was extracted with ethyl acetate. The organic phase was successively washed with water (50 mL) and brine (50 mL) and then dried over anhydrous sodium sulfate. From the organic phase, the solvent was removed by evaporation under reduced pressure and the resultant residue was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=80:20 to 70:30). From the eluted solution, the solvent was removed by evaporation under reduced pressure to give the title compound (3.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040525B2
Source datasetuspto-grants-2015_05
ORD IDord-ac5c2ffb162c4fcc90a02d38236125b9
Source noteuspto-grants-2015_05