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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261094Generated: November 3, 2026

Potassium Hydroxide → 3-Bromo-benzofuran-5-carbaldehyde

https://huagongshe.com/reaction/2261094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2,3-Dibromo-2,3-dihydro-1-benzofuran-5-carbaldehydeHCID 57469664—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product3-Bromo-benzofuran-5-carbaldehydeHCID 5746966396.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 2,3-dibromo-2,3-dihydro-1-benzofuran-5-carbaldehyde (4.1 g) in dry ethanol (15 mL) was added a solution of KOH (2.2 eq.) in dry ethanol (14 mL) and refluxed at 70° C. for 1 h. The reaction mixture was cooled, diluted with water and extracted with EtOAc (3×50 mL). The organic layer was washed with water, brine and dried. The solvent was removed under vacuum and the residue was purified by flash chromatography (pet. ether/EtOAc 99.5:0.5) to give the title compound as a pale yellow solid (2.91 g (80% pure), yield=78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846925B2
Source datasetuspto-grants-2010_12
ORD IDord-536903aa5f574ebc9f6f46b5770fc5cd
Source noteuspto-grants-2010_12