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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376974Generated: October 31, 2026

Allyl bromide → 4-Acetoxy-3,5-di-tert-butyl-1-(2-propenyloxy)benzene

https://huagongshe.com/reaction/1376974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-DI-Tert-butyl-4-hydroxyphenyl acetateHCID 11139998—
SolventAcetoneHCID 180—
Product4-Acetoxy-3,5-di-tert-butyl-1-(2-propenyloxy)benzeneHCID 11088037—

Reaction Steps

4-Acetoxy-3,5-di-tert-butylphenol (10 g) and potassium carbonate (15.6 g) were dissolved in acetone (300 ml). After addition of 3-bromo-1-propene (6.55 ml), the mixture was refluxed for 24 h. The reaction mixture was concentrated under reduced pressure and water was added to the concentrate. The mixture was subjected to extraction with diethyl ether and the organic layer was washed with water and saturated brine, then dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (10% ethyl acetate in n-hexane) to afford 4-acetoxy-3,5-di-tert-butyl-1-(2-propenyloxy)benzene (11 g) as a colorless liquid in a quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663373
Source datasetuspto-grants-1997_09
ORD IDord-92915a9a68214567ae98903390062a93
Source noteuspto-grants-1997_09