HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717101Generated: October 30, 2026
Potassium Iodide → HCID 123949802, compound
https://huagongshe.com/reaction/717101
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methylbenzimidazole | HCID 11984 | — |
| Reactant | 2-(4-(Bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 3734506 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 123949802 | HCID 123949802 | 35.4% |
Reaction Steps
To a solution of 4-bromomethylphenylboronic acid pinacol ester (564 mg, 1.90 mmol) in acetone (19 mL) was added 2-methylbenzimidazole (377 mg, 2.85 mmol), potassium iodide (16 mg, 0.095 mmol) and K2CO3 (394 mg, 2.85 mmol) and the reaction mixture heated at 60° C. for 3.25 h. The reaction mixture was diluted with H2O and extracted with EtOAc (×2). The organic layers were combined, dried (phase separation cartridge) and concentrated in vacuo. The crude material was purified by reverse phase preparative HPLC-MS to afford 2-Methyl-1-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzyl]1H-benzoimidazole as an off-white solid (234 mg, 35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193689B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-628d8f0532dc4d829fdcbb36d8d413c5 |
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| Source note | uspto-grants-2015_11 |
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