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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960135Generated: October 31, 2026

3-Bromophenol → 5-Biphenyl-4-yl-2-(3-bromo-phenoxy)-6-fluoro-1H-benzoimidazole

https://huagongshe.com/reaction/1960135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromophenolHCID 11563—
Reactant5-Biphenyl-4-yl-6-fluoro-2-methanesulfonyl-1H-benzoimidazoleHCID 67445536—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
Product5-Biphenyl-4-yl-2-(3-bromo-phenoxy)-6-fluoro-1H-benzoimidazoleHCID 67446383—

Reaction Steps

To a solution of compound 13-6 (1.53 g, 4.2 mmol) in 20 mL in pyridine was added 3-bromo-phenol (1.4 g, 8.4 mmol). The reaction mixture was heated to reflux and allowed to stir for 48 h. The reaction mixture was diluted with EtOAc (150 mL) and washed three times with 100 mL portions of saturated aqueous ammonium chloride. The combined organic layers were dried over MgSO4 filtered and concentrated in vacuo. The crude was purified on ISCO (EtOAc/Hexanes=1/1) to yield the title compound 13-7 along with recovered starting material 13-6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410284B2
Source datasetuspto-grants-2013_04
ORD IDord-c5406b9f3fb74ecf9963fcda22d5b0d8
Source noteuspto-grants-2013_04