HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Benzofuran, 5-bromo-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-(4-bromo-2-formylphenoxy)acetic acid | HCID 968879 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Benzofuran, 5-bromo- | HCID 90015 | 40% |
Reaction Steps
To a mixture of 2-formyl-4-bromophenoxy acetic acid (50 g, 0.192 mol), sodium acetate (100 g, 1.21 mol) in acetic acid (250 mL) at 100° C. was added acetic anhydride (100 mL) portions during a period of 3 h. The reaction mixture was then refluxed for 20 h. The solvent was removed by distillation and residue diluted with 3N HCl (500 mL) and refluxed for 2 h. The reaction mixture was then concentrated under vacuum and product extracted with pet. ether (3×200 mL). The organic layer was washed with 10% NaHCO3 solution and evaporated to give 5-bromo-1-benzofuran (15 g, 40%) as a pale yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07846925B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-115187c9d5c94aec858b0e67b7151d76 |
| Source note | uspto-grants-2010_12 |