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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172778Generated: November 2, 2026

Hydrochloric Acid → (1,2-diphenyl-1H-benzimidazol-5-yl)Boronic acid

https://huagongshe.com/reaction/1172778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
Reactant5-bromo-1,2-diphenyl-1H-benzo[d]imidazoleHCID 23094059—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(1,2-diphenyl-1H-benzimidazol-5-yl)Boronic acidHCID 2316023335.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

In an argon atmosphere, 10 g (29 mmol) of 5-bromo-1,2-diphenyl-1H-benzimidazole were dissolved into 100 mL of dehydrated THF, and the temperature of the solution was cooled to −78° C. Then, 20 mL of n-butyllithium (in hexane, 1.6 mol/L) were dropped. After the mixture had been stirred at −78° C. for 1 hour, the temperature of the mixture was increased to 0° C. The temperature of the mixture was cooled to −78° C. again, and 9.7 mL (87 mmol) of trimethoxyborane were dropped. The mixture was stirred at −78° C. for 1 hour, and was then stirred at room temperature for 2 hours. 100 mL of 10-mass % hydrochloric acid were added, and the whole was stirred for 1 hour, followed by filtration. The organic layer of the filtrate was washed with a saturated sodium chloride solution and dried with magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by means of silica gel column chromatography to obtain 3.2 g of 1,2-diphenyl-1H-benzimidazole-5-boronic acid (35% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833632B2
Source datasetuspto-grants-2010_11
ORD IDord-dc72c64157954013abaa0af8c288f3ca
Source noteuspto-grants-2010_11