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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774280Generated: November 3, 2026

Hydrochloric Acid → Dibenzo(b,d)furan-2-ylboronic Acid (contains varying amounts of Anhydride)

https://huagongshe.com/reaction/1774280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-BromodibenzofuranHCID 6856—
ReactantTrimethyl borateHCID 8470—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductDibenzo(b,d)furan-2-ylboronic Acid (contains varying amounts of Anhydride)HCID 1203237671.7%

Reaction Conditions

Temperature-40 °C

Reaction Steps

Under an argon atmosphere, 24.7 g of 2-bromodibenzofuran and 400 ml of anhydrous THF were loaded into a 1,000-ml three-necked flask, and then 63 ml of a solution of n-butyllithium in hexane having a concentration of 1.6 M were added to the mixture during the stirring of the mixture at −40° C. The reaction solution was stirred for 1 hour while being heated to 0° C. The reaction solution was cooled to −78° C. again, and then a solution of 26.0 g of trimethyl borate in 50 ml of dry THF was dropped to the solution. The reaction solution was stirred at room temperature for 5 hours. 200 milliliters of 1N hydrochloric acid were added to the solution, and then the mixture was stirred for 1 hour. After that, the aqueous layer was removed. The organic layer was dried with magnesium sulfate, and then the solvent was removed by distillation under reduced pressure. The resultant solid was washed with toluene. Thus, 15.2 g of dibenzofuran-2-boronic acid were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260390B2
Source datasetuspto-grants-2016_02
ORD IDord-651f4a49481247f1860fc945b5f8d188
Source noteuspto-grants-2016_02