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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74204Generated: October 29, 2026

Acetaldehyde → 5-(Benzoxazol-2-yl)-1-(4-fluorophenyl)-2-methylbenzimidazole

https://huagongshe.com/reaction/74204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant2-(2-(4-Fluorophenyl)aminoanilin-5-yl)benzoxazoleHCID 67498132—
SolventDimethylformamideHCID 6228—
Product5-(Benzoxazol-2-yl)-1-(4-fluorophenyl)-2-methylbenzimidazoleHCID 6749817449%

Reaction Steps

To a solution of 2-(2-(4-fluorophenyl)aminoanilin-5-yl)benzoxazole (see Working Example 34-1) (38.0 mg, 0.119 mmol) in dimethylformamide (2 mL) was added an aqueous solution of acetaldehyde (approx. 90%, 22.6 μL, 0.360 mmol) and oxone (73.2 mg, 0.119 mmol), and this was stirred at room temperature for 3 hours. After the reaction was complete, aqueous potassium carbonate solution was added, this was filtered and washed with water. The crystals obtained were purified by silica gel column chromatography to yield the title compound (20.0 mg, 49% yield) as light brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-ba05cdd7cd0a4be1a10844316c68f610
Source noteuspto-grants-2014_09