HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52656Generated: October 26, 2026
Potassium Persulfate → 4-Bromo-2,3-dihydro-2,2-dimethyl-3-benzofuranone
https://huagongshe.com/reaction/52656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Persulfate | HCID 24412 | — |
| Reactant | 4-Bromo-2,2-dimethyl-2,3-dihydrobenzofuran | HCID 53989127 | — |
| Catalyst | Copper sulfate pentahydrate | HCID 24463 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Bromo-2,3-dihydro-2,2-dimethyl-3-benzofuranone | HCID 54377906 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616718 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-3fbbd22283364d73a3e65ae42d09c7e0 |
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| Source note | uspto-grants-1997_04 |
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