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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 363789Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/363789

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 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05874579
Quelldatensatzuspto-grants-1999_02
ORD IDord-5a9cfecf7cdd4829b90d7bb4c1e90f3e
Quellennotizuspto-grants-1999_02