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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484633Generated: October 26, 2026

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

https://huagongshe.com/reaction/484633

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 numberUS05231182
Source datasetuspto-grants-1993_07
ORD IDord-c4afa18686dc4973a4e4f78e181ea41b
Source noteuspto-grants-1993_07