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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407449Generated: October 30, 2026

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

https://huagongshe.com/reaction/2407449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
Reactant1-Benzofuran-5-carbonitrileHCID 2795184—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(5-Cyano-1-benzofuran-2-yl)boronic acidHCID 66787891—

Reaction Steps

To benzofuran-5-carbonitrile (500 mg, 3.49 mmol) in THF (9.98 mL) at −78° C. was added nBuLi 1.6M in hexanes (2.401 mL, 3.84 mmol) dropwise. The mixture was stirred for 30 min at this temperature, and then trimethyl borate (0.858 mL, 7.68 mmol) was added dropwise. The mixture was stirred for 20 min, and then HCl 2N (11.52 mL, 23.05 mmol) was added. The bath was removed, and stirring continued for 30 min. The mixture was diluted with water and extracted with EtOAc three times, dried over magnesium sulfate, filtered, concentrated. Crude 5-cyanobenzofuran-2-ylboronic acid (623 mg, 87%) was then dried and used as is for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809545B2
Source datasetuspto-grants-2014_08
ORD IDord-ab00fe142148405bb3b9830518663a29
Source noteuspto-grants-2014_08