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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483560Generated: October 25, 2026

Pyridine → N-[3-(Hydroxymethyl)phenyl]-4-(tetradecyloxy)benzamide

https://huagongshe.com/reaction/483560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloroformHCID 6212—
Reactant3-Aminobenzyl alcoholHCID 80293—
ReactantBenzoyl chloride, 4-(tetradecyloxy)-HCID 9998158—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-[3-(Hydroxymethyl)phenyl]-4-(tetradecyloxy)benzamideHCID 1000333382.1%

Reaction Steps

To a solution of 8.17 g of m-aminobenzyl alcohol and 16.14 g of pyridine in 200 ml of methylene chloride is added at 0° C. over 30 minutes a solution of 18 g of p-tetradecyloxybenzoyl chloride in 200 ml of methylene chloride. Stirring is continued for another 6 hours. An additional 400 ml of chloroform and water is added followed by warming to dissolve all the solids. The warm organic layer is separated and washed with dilute hydrochloric acid and saturated sodium bicarbonate. The warm organic layer is dried and filtered. The filtrate is diluted with an equal volume of hexane and cooled in a refrigerator overnight. The resulting solid is collected and air dried to give 18.4 g of the desired product as a white solid, m.p. 112°-115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05225425
Source datasetuspto-grants-1993_07
ORD IDord-ee6686cdafc5499fad2c7154160a53da
Source noteuspto-grants-1993_07