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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378571Generated: October 27, 2026

Imidazole → 3-Bromo-4-(1H-imidazol-1-YL)benzaldehyde

https://huagongshe.com/reaction/2378571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantChloroformHCID 6212—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-4-fluorobenzaldehydeHCID 173604—
SolventMethanolHCID 887—
Product3-Bromo-4-(1H-imidazol-1-YL)benzaldehydeHCID 5342959064%

Reaction Steps

According to the procedure described in the synthesis method of Intermediate Int. n-26 (Synthesis method NG) provided that the reaction was performed for 20 hours, and the column chromatography was performed with chloroform:methanol=100:1, 3-bromo-4-fluorobenzaldehyde (1.246 g, TCI), potassium carbonate (825.1 mg) and imidazole (444 mg, TCI) were reacted and treated to obtain the title compound (Intermediate Int. n-32, 986.1 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470807B2
Source datasetuspto-grants-2008_12
ORD IDord-cb2af22aaeee432ebc6b209939b7ee4c
Source noteuspto-grants-2008_12