Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030516Generated: October 28, 2026

Benzaldehyde → HCID 178432167, compound

https://huagongshe.com/reaction/1030516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178432166HCID 178432166—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 178432167HCID 1784321671.6%

Reaction Steps

A mixture of 3.8 g (0.026 mol) 4-amino-2-methylbenzimidazole, 2.7 g (0.026 mol) benzaldehyde and 0.05 g paratoluene sulfonic acid in 250 ml toluene was refluxed and the water formed was separated during 20 h. Upon cooling the volatiles were removed under reduced pressure. The residue obtained was suspended in 150 ml methanol and 1.8 g (0.048 mol) NaBH4 was added. The mixture was stirred at room temperature for 2 h and methanol was removed under reduced pressure. The residue was dissolved in methylene chloride, washed with water and dried (Na2SO4). After filtration, methylene chloride was removed under reduced pressure. Chromatography on silica gel and elution with methylene chloride:methanol (10:1) gave 0.1 g (0.00042 mol) of 4-benzylamino-2-methyl benzimidazole

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106862
Source datasetuspto-grants-1992_04
ORD IDord-cc54039658e04c728d79add1bdba706f
Source noteuspto-grants-1992_04