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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 484592Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/484592

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktChloroformHCID 6212—
Edukt3-Aminobenzyl alcoholHCID 80293—
EduktBenzoyl chloride, 4-(tetradecyloxy)-HCID 9998158—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[3-(Hydroxymethyl)phenyl]-4-(tetradecyloxy)benzamideHCID 1000333382,1%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05231182
Quelldatensatzuspto-grants-1993_07
ORD IDord-1d0883649c7d424994873662eac1dba4
Quellennotizuspto-grants-1993_07