Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461939Generated: October 29, 2026

Pyridine → N-[4-(Hydroxymethyl)phenyl]-4-(tetradecyloxy)benzamide

https://huagongshe.com/reaction/1461939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Aminobenzyl alcoholHCID 69331—
ReactantBenzoyl chloride, 4-(tetradecyloxy)-HCID 9998158—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductN-[4-(Hydroxymethyl)phenyl]-4-(tetradecyloxy)benzamideHCID 1041095867.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 9.75 g of p-aminobenzyl alcohol and 19.27 g of pyridine in 230 ml of methylene chloride cooled to 0° C. is added over 35 minutes a solution of 21.5 g of 4-tetradecyloxybenzoyl chloride in 230 ml of methylene chloride. The mixture is stirred at room temperature for 2 hours and diluted with chloroform. The mixture is heated to dissolve insolubles, washed with hot water and hot dilute hydrochloric acid then dried. The mixture is filtered hot and the solvent evaporated to a residue which is crystallized from tetrahydrofuran:hexane to give 18.1 g of the desired product as a yellow powder, m.p. 140°-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05077409
Source datasetuspto-grants-1991_12
ORD IDord-cc7b3523a3db4d74b1c9406ab7c0f80c
Source noteuspto-grants-1991_12