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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850468Generated: October 25, 2026

Dimethylformamide → Bis[2-(4-pyridyl)ethyl]amine

https://huagongshe.com/reaction/850468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1-BromopentaneHCID 8057—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Hydroxy-4-methoxy-2-nitrobenzaldehydeHCID 221191—
Reactant5-Hydroxy-4-methoxy-2-nitrobenzaldehydeHCID 285294—
SolventWaterHCID 962—
SolventEthyl acetate hexaneHCID 21226206—
ProductBis[2-(4-pyridyl)ethyl]amineHCID 416637—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-hydroxy4-methoxy-2-nitrobenzaldehyde and 3-hydroxy4-methoxy-6-nitrobenzaldehyde, and DMF (700 ml) were mixed, and potassium carbonate (136.7 mg, 989 mmol) and bromopentane (122.7 ml, 989 mmol) were successively added to this solution. The reaction mixture was stirred at 100° C. for 4 hours and fltered. Water (600 ml) and hexane-ethyl acetate (1:1, 600 ml) were added to the filtrate for separation. The aqueous layer was extracted with hexane-ethyl acetate (1:1, 600 ml). The organic layers were combined, and dried over anhydrous magnesium sulfate. The drying agent was filtered off, and the filtrate was evaporated. The precipitated crystals were collected by filtration to give 4-methoxy-6-nitro-3-pentyloxybenzaldehyde (2)) (90.1 g, 44%) as yellow crystals. The filtrate after filtration of said crystals was further evaporated to give 4-methoxy-2-nitro-3-pentyloxybenzaldehyde (1) (117 g, 58%) as a red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017919
Source datasetuspto-grants-2000_01
ORD IDord-469c72f457f440e9a1fdabf715508a43
Source noteuspto-grants-2000_01