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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705012Generated: October 29, 2026

4-Chlorophenylboronic acid → HCID 86303660, compound

https://huagongshe.com/reaction/705012

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorophenylboronic acidHCID 74299—
ReactantFuran-2-boronic acidHCID 2734357—
ReactantHCID 66520703HCID 66520703—
ReactantHCID 178418934HCID 178418934—
ProductHCID 86303660HCID 8630366012%

Reaction Steps

The procedure described above for Formula Ic-iii in Example 16 was followed, starting from 4-chloro-phenylboronic acid and 4-bromo-1H-imidazole, to prepare 4-bromo-1-(4-chlorophenyl)-1H-imidazole, which was then reacted with furan-2-ylboronic acid to prepare the desired 1-(4-chlorophenyl)-4-(furan-2-yl)-1H-imidazole (15 mg, 0.061 mmol, yield 12%) as an off-white solid. The HPLC purity of the final product was 95.45%. LC-MS [M+H] 245 (C13H9ClN2O+H expected 245.04). The 1H-NMR spectra was in accordance with the chemical structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173401B2
Source datasetuspto-grants-2015_11
ORD IDord-a819c51ed2294574b4b70bb3911a5077
Source noteuspto-grants-2015_11