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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261073Generated: November 1, 2026

Acetic Anhydride → Benzofuran, 5-bromo-

https://huagongshe.com/reaction/2261073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium AcetateHCID 517045—
Reactant2-(4-bromo-2-formylphenoxy)acetic acidHCID 968879—
SolventAcetic AcidHCID 176—
ProductBenzofuran, 5-bromo-HCID 9001540%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846925B2
Source datasetuspto-grants-2010_12
ORD IDord-115187c9d5c94aec858b0e67b7151d76
Source noteuspto-grants-2010_12