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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247967Generated: October 25, 2026

Pyridine → N-[2-(2-Pyridinyl)ethyl]-4-(tetradecyloxy)benzamide

https://huagongshe.com/reaction/247967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-PyridineethanamineHCID 75919—
ReactantBenzoyl chloride, 4-(tetradecyloxy)-HCID 9998158—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductN-[2-(2-Pyridinyl)ethyl]-4-(tetradecyloxy)benzamideHCID 1047831441.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° solution of 2.54 g of 2-(2-aminoethyl)pyridine, 50 ml of methylene chloride and 6.42 ml of pyridine is added, dropwise, 7.0 g of product from Example 3 in 250 ml of methylene chloride. The reaction is stirred at 0° C. for 2 hours followed by 14 hours at room temperature. The reaction is diluted with chloroform, washed with saturated sodium bicarbonate, water and saturated sodium chloride, dried and concentrated in vacuo. The residue is purified by column chromatography (silica gel:75-100% ethyl acetate/hexane) to give 3.58 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05208247
Source datasetuspto-grants-1993_05
ORD IDord-3d766805a00346a79f60fb0a4ee3c4ec
Source noteuspto-grants-1993_05