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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728840Generated: October 26, 2026

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

https://huagongshe.com/reaction/1728840

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 numberUS05328921
Source datasetuspto-grants-1994_07
ORD IDord-826937f8079745a4834aeb9859baf48a
Source noteuspto-grants-1994_07