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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734618Generated: November 1, 2026

Potassium Persulfate → 4-Bromo-2,3-dihydro-2,2-dimethyl-3-benzofuranone

https://huagongshe.com/reaction/1734618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium PersulfateHCID 24412—
Reactant4-Bromo-2,2-dimethyl-2,3-dihydrobenzofuranHCID 53989127—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product4-Bromo-2,3-dihydro-2,2-dimethyl-3-benzofuranoneHCID 5437790667%

Reaction Steps

Under a nitrogen atmosphere, a stirred solution of 3.0 grams (0.013 mole) 4-bromo-2,3-dihydro-2,2-dimethylbenzofuran, 10.7 grams (0.039 mole) of potassium persulfate, and 3.3 grams (0.013 mole) of copper(II) sulfate pentahydrate in 30 mL of water and 30 mL of acetonitrile was heated at reflux for one hour. After this time the reaction mixture was poured into 200 mL of water. The mixture was then extracted with one 200 mL portion of diethyl ether. The extract was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residual oil. The oil was subjected to column chromatography on silica gel. Elution was accomplished using 1:1 petroleum ether and methylene chloride. The product-containing fractions were combined and concentrated under reduced pressure, yielding 2.1 grams of 4-bromo-2,3-dihydro-2,2-dimethyl-3-benzofuranone. The NMR spectrum was consistent with the proposed structure. Steps A through C were repeated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534518
Source datasetuspto-grants-1996_07
ORD IDord-1de5a8b7738549beb5dcc6b37543f20d
Source noteuspto-grants-1996_07