Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902459Generated: November 2, 2026

Benzaldehyde → 3-(1H-Benzimidazol-1-yl)-N-benzylpropan-1-amine

https://huagongshe.com/reaction/1902459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant3-(1H-1,3-benzodiazol-1-yl)propan-1-amineHCID 3920849—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-(1H-Benzimidazol-1-yl)-N-benzylpropan-1-amineHCID 20469054—

Reaction Steps

0.5 Gram of 10% palladium on charcoal was prehydrogenated in 100 ml. of absolute ethanol until the uptake of hydrogen stopped. Then, a solution of 10 grams of 1H-benzimidazole-1-propanamine and 6.7 grams of benzaldehyde in 50 ml. of absolute ethanol was added and the mixture was stirred at atmospheric pressure and room temperature under hydrogen until the calculated amount of hydrogen was taken up. The catalyst was then removed by filtration and the solvent was evaporated to leave N-benzyl-1H-benzimidazole-1-propanamine as a colorless oil. This material was sufficiently pure for further reaction but, if desired, a pure sample could be obtained by column chromatography on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04363808
Source datasetuspto-grants-1982_12
ORD IDord-5ab23850e9a44aa79a3e87306aef8c55
Source noteuspto-grants-1982_12