Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,3-Dibromo-2,3-dihydrobenzofuran | HCID 12394037 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Bromo-1-benzofuran | HCID 640589 | 108% |
Reaction Steps
To 11.3 g KOH (176 mmol) in 100 mL ethanol at 0° C. was added in small portions 22.2 g of 2,3-dibromo-2,3-dihydrobenzofuran, and the resulting reaction mixture was stirred at 0° C. for an additional 3 h. Most of the solvent was then removed in vacuo. Water and ether were added to the residue. The aq layer was separated and extracted with ether. The combined ether layers were washed with water and brine, dried (MgSO4), and concentrated to give 17 g of 3-bromobenzofuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994270 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-2265f6c0f21e4725bfa14457e4adc82c |
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| Source note | uspto-grants-1999_11 |
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