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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 233605Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/233605

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium PersulfateHCID 24412—
Edukt4-Bromo-2,2-dimethyl-2,3-dihydrobenzofuranHCID 53989127—
KatalysatorCopper sulfate pentahydrateHCID 24463—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-Bromo-2,3-dihydro-2,2-dimethyl-3-benzofuranoneHCID 5437790667%

Reaktionsschritte

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 is heated at reflux for one hour. After this time the reaction mixture is poured into 200 mL of water. The mixture is then extracted with one 200 mL portion of diethyl ether. The extract is dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure to a residual oil. The oil is subjected to column chromatography on silica gel. Elution is accomplished using 1:1 petroleum ether and methylene chloride. The product-containing fractions are combined and concentrated under reduced pressure, yielding 2.1 grams of 4-bromo-2,3-dihydro-2,2-dimethyl-3-benzofuranone. The NMR spectrum is consistent with the proposed structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05593998
Quelldatensatzuspto-grants-1997_01
ORD IDord-716fca5737634edf92985c70a3636402
Quellennotizuspto-grants-1997_01