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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728836Generated: October 26, 2026

Pyridine → N-(2-Pyridinylmethyl)-4-(tetradecyloxy)benzeneacetamide

https://huagongshe.com/reaction/1728836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-PyridinemethanamineHCID 19509—
Reactantp-TetradecyloxyphenylacetylchlorideHCID 10021844—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductN-(2-Pyridinylmethyl)-4-(tetradecyloxy)benzeneacetamideHCID 1036588061.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. solution of 4.64 g of 2-(aminomethyl)pyridine, 13.2 ml of pyridine and 50 ml of methylene chloride is added, dropwise, 15 g of product from Example 53 in 150 ml of methylene chloride. The reaction is stirred at 0° C. for 1 hour followed by 18 hours at room temperature. The reaction is diluted with chloroform, washed with sodium bicarbonate, water and saturated sodium chloride, dried and concentrated in vacuo. The residue is purified by column chromatography (silica ge1:75-100% ethyl acetate/hexane) to give 11.0 g of the desired product as colorless prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05328921
Source datasetuspto-grants-1994_07
ORD IDord-8371e7ff438841bea1f0fb6598dcc403
Source noteuspto-grants-1994_07