HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-Bromo-7-fluoro-1-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 15158727 | HCID 15158727 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Bromo-7-fluoro-1-benzofuran | HCID 15158728 | 97.6% |
Reaction Steps
To a solution of potassium hydroxide (12.7 g) in ethanol (180 ml) was slowly added the product obtained in Step 1 (34 g) and stirred for 3 hours. The resulting solution was neutralized by acetic acid, then extracted with ether. The organic layer was washed with successive water and saturated aqueous NaCl solution. After drying over anhydrous sodium sulfate, ether was removed in vacuo to give 24.1 g of the objective compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE035279 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-1c00bc0a59c447589405176ba475b378 |
| Source note | uspto-grants-1996_06 |