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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2302320Generated: November 1, 2026

Benzaldehyde → HCID 3155259, compound

https://huagongshe.com/reaction/2302320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant1H-Imidazole-1-propanamineHCID 78736—
ReactantSodium AcetateHCID 517045—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 3155259HCID 315525992.4%

Reaction Steps

A mixture of 1-(3-aminopropyl)imidazole (Aldrich, 37.1 g, 297 mmol), benzaldehyde (30 g, 283 mmol), 3 Å molecular sieves (50 g), sodium acetate (24.1 g, 283 mmol) and anhydrous methanol (700 mL) are stirred at room temperature under N2 overnight. The mixture is cooled to 0° C. and sodium borohydride (10.9 g, 288 mmol) is added portionwise over 1 hour. The mixture is stirred at room temperature for 3 hours. The mixture is filtered through celite, washed with methanol, and concentrated in vacuo to give a residue which is diluted with dichloromethane and washed with 10% aqueous sodium hydroxide. The organic phases are washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to give the title compound as a pale yellow oil (56.3 g, MH+=216).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432959B1
Source datasetuspto-grants-2002_08
ORD IDord-d4632895d9504fc19f7c36f088ab8cd7
Source noteuspto-grants-2002_08