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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452358Generated: November 3, 2026

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

https://huagongshe.com/reaction/1452358

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 numberUS05606089
Source datasetuspto-grants-1997_02
ORD IDord-e05628a256bd4394ad45761b1a9e2b13
Source noteuspto-grants-1997_02