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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893108Generated: October 26, 2026

Hydrochloric Acid → 2,3-Diphenylbenzo[b]furan-6-boronic acid

https://huagongshe.com/reaction/1893108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
Reactant6-Bromo-2,3-diphenylbenzofuranHCID 59866501—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2,3-Diphenylbenzo[b]furan-6-boronic acidHCID 5986651060%

Reaction Conditions

Temperature-40 °C

Reaction Steps

Under an argon atmosphere, 400 mL of anhydrous THF were added to 40.2 g of 6-bromo-2,3-diphenylbenzo[b]furan, and the mixture was stirred at −40° C. During the stirring, 72 mL of a 1.6-M solution of n-butyllithium in hexane were added to the mixture. The reaction solution was stirred for 1 hour while being heated to 0° C. The reaction solution was cooled to −78° C. again, and a solution of 54.0 g (250 mmol) 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 mL of 1N hydrochloric acid were added to the reaction solution, and the mixture was stirred for 1 hour. After that, the water layer was removed. The organic layer was dried with magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The resultant solid was washed with toluene, whereby 21.7 g of 2,3-diphenylbenzo[b]furan-6-boronic acid were obtained (60% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08512875B2
Source datasetuspto-grants-2013_08
ORD IDord-9e838d81e1d74c73a26f061d92b09f21
Source noteuspto-grants-2013_08