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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262438Generated: November 3, 2026

HCID 23094072, compound → HCID 23094067, compound

https://huagongshe.com/reaction/2262438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23094072HCID 23094072—
SolventO-XyleneHCID 7237—
ProductHCID 23094067HCID 2309406790%

Reaction Steps

Suspending 3.6 g (12 mmol) of 5′-bromo-2′-(N-phenylamino)-acetanilide obtained in the above step (1) into 30 milliliter of xylene, and adding 0.68 g (3.6 mmol) of p-toluenesulfonic acid 1 hydrate, the resultant solution was azeotropically dehydrated while refluxing with heating for 5 hours. The reacted solution was cooled down to room temperature, and the solvent was removed by distillation. Dissolving the resultant solid into ethyl acetate, and after sequentially washing with water, with 10% potassium carbonate aqueous solution and with saturated solution of sodium chloride, it was dried with sulfuric anhydride magnesium, followed by removing the solvent by distillation under reduced pressure, 3.0 g of 5-bromo-2-methyl-1-phenyl-1H-benzimidazole was obtained (yield: 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851071B2
Source datasetuspto-grants-2010_12
ORD IDord-b0be6259e8de4560bb2a55b769cd18d9
Source noteuspto-grants-2010_12