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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359968Generated: November 3, 2026

Hydrogen Peroxide → HCID 10921072, compound

https://huagongshe.com/reaction/359968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSulfuric AcidHCID 1118—
ReactantPeracetic AcidHCID 6585—
Reactant4-Ethenylphenyl acetateHCID 75821—
ReactantSodium AcetateHCID 517045—
CatalystSulfuric AcidHCID 1118—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHCID 10921072HCID 1092107298%

Reaction Steps

Commercially available peracetic acid (57 g) produced by the oxidation of acetic acid with hydrogen peroxide using sulfuric acid as catalyst, and containing about 35 wt % of peracetic acid, about 19 wt % of water, about 0.6 wt % of hydrogen peroxide, about 1 wt % of sulfuric acid, and the remainder acetic acid, is mixed with chloroform (250 ml) and transferred to a separatory funnel. The upper aqueous layer is discarded and the chloroform layer is dried over magnesium sulfate and filtered to yield a solution containing about 37 wt % of peracetic acid, about 0.6% wt of hydrogen peroxide, and the remainder acetic acid. No more than a trace of sulfuric acid or water is detectable. The solution is added dropwise to an ice cold solution of 4-acetoxystyrene (24.3 g, 0.15 mol) in chloroform (150 ml) containing sodium acetate (5.0 g). After the addition of peracetic acid solution, the reaction mixture is warmed up to room temperature and stirred overnight. The reaction mixture is washed with water (3×200 ml) and saturated sodium bicarbonate solution (3×200 ml), dried over anhydrous magnesium sulfate, filtered, and concentrated in-vacuo to afford an oil characterized by NMR analysis as 4-acetoxystyrene oxide (26.2 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05003115
Source datasetuspto-grants-1991_03
ORD IDord-b0690a4daaea429f95235211feebaa22
Source noteuspto-grants-1991_03