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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74197Generated: October 29, 2026

Acetaldehyde → 5-(Benzoxazol-2-yl)-2-methyl-1-tert-butylbenzimidazole

https://huagongshe.com/reaction/74197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant2-(2-Tert-butylaminoanilin-5-yl)benzoxazoleHCID 67498414—
SolventDimethylformamideHCID 6228—
Product5-(Benzoxazol-2-yl)-2-methyl-1-tert-butylbenzimidazoleHCID 6749792338%

Reaction Steps

To a solution of 2-(2-tert-butylaminoanilin-5-yl)benzoxazole (see Working Example 29-1) (45.0 mg, 0.160 mmol) in dimethylformamide (2 mL) was added an aqueous solution of acetaldehyde (approx. 90%, 235 μL, 0.480 mmol) and oxone (63.9 mg, 0.104 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 (18.2 mg, 38% yield) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-2c534f3886654c50aba4cc10635778be
Source noteuspto-grants-2014_09