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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503142Generated: October 29, 2026

Hydrochloric Acid → (5-Fluoro-1-benzofuran-2-yl)boronic acid

https://huagongshe.com/reaction/503142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethyl borateHCID 9009—
Reactant5-Fluoro-1-benzofuranHCID 11788322—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product(5-Fluoro-1-benzofuran-2-yl)boronic acidHCID 22260896—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a nitrogen atmosphere, to a solution of 2.0 g of 5-fluorobenzofuran in 150 ml tetrahydrofuran was added 18.5 ml of a 1.59 M solution of n-butyllithium in n-hexane at −78° C., and the mixture was stirred at the same temperature for 10 minutes and at 0° C. for further 10 minutes. At −78° C., 3.7 ml of triethoxyborane was added, and the mixture was stirred for 2 hours while elevating to 0° C. 30 ml of 1 N hydrochloric acid was added, stirred at room temperature for 1 hour, and then the mixture was extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and the solvent was evaporated. The crude product was purified and separated by silica gel column chromatography (ethyl acetate:n-hexane=1:3 to 1:1), to give 525 mg of the title compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776890B2
Source datasetuspto-grants-2010_08
ORD IDord-681b468dd8404569907bf83eda08558e
Source noteuspto-grants-2010_08