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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383978Generated: October 26, 2026

Sodium Bicarbonate → 5-Bromo-2-fluoro-1-benzofuran

https://huagongshe.com/reaction/383978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant5-Bromo-2-benzofurancarboxylic acidHCID 735247—
ReactantSelectfluorHCID 2724933—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
Product5-Bromo-2-fluoro-1-benzofuranHCID 57439113—

Reaction Steps

5-Bromobenzofuran-2-carboxylic acid (4.68 g) was suspended in carbon tetrachloride (150 ml) and water (50 ml). To this was added sodium bicarbonate (3.36 g), followed by Selectflor (7.1 g) and the reaction mixture was stirred rapidly for 20 hours. The reaction mixture was diluted with dichloromethane and 2N sodium hydroxide solution. The organic phase was separated, washed with brine and dried over anhydrous MgSO4. The solvent was evaporated under reduced pressure at room temperature. The residue was applied to a silica cartridge (20 g) and eluted with diethyl ether. This gave 5-bromo-2-fluoro-1-benzofuran (1.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367673B2
Source datasetuspto-grants-2013_02
ORD IDord-8f6c897831ea4099a94df7738e852e15
Source noteuspto-grants-2013_02