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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 5-bromo-1,2-diphenyl-1H-benzo[d]imidazole | HCID 23094059 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1,2-diphenyl-1H-benzimidazol-5-yl)Boronic acid | HCID 23160233 | 35.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07833632B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-dc72c64157954013abaa0af8c288f3ca |
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| Source note | uspto-grants-2010_11 |
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