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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 463750Erstellt: 25. Oktober 2026

Sodium Hydroxide → 9,12-Octadecadienamide, N-((4-hydroxy-3-methoxyphenyl)methyl)-, (E,E)-

https://huagongshe.com/reaction/463750

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktPhenol, 4-(aminomethyl)-2-methoxy-, hydrochloride (1:1)HCID 165576—
Edukt9,12-Octadecadienoyl chloride, (9Z,12Z)-HCID 5365578—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt9,12-Octadecadienamide, N-((4-hydroxy-3-methoxyphenyl)methyl)-, (E,E)-HCID 6507149—
ProduktOctadecadienamideHCID 54225156—

Reaktionsschritte

N-vanillyl-(E,E)-9,12-octadecadienamide was synthesized by the following method: ##STR5## Specifically 6.88 g of 4-hydroxy-3-methoxybenzylamine-HCl was dissolved in 50 ml of tetrahydrofuran (THF), and stirred. Added were 14 ml of a 5N solution of NaOH, and the mixture was stirred for 10 to 15 minutes. Then 10.6 g of (E,E)-9,12 octadecadienoyl chloride (linoelaidoyl chloride), dissolved in THF, was added dropwise. The mixture was then stirred overnight, allowing it to come to room temperature. The solvent was evaporated and the residue partitioned between ethyl ether and water. The organic phase extract was washed with HCl, sodium bicarbonate, water, and brine, and then dried and filtered. 16 g of crude N-vanillyl-(E,E)-9,12)-octadecadienamide was obtained. Purification by recrystallization from ether and pentane gave 9.4 g of analytically pure product. Its structure was confirmed via nuclear magnetic resonance and infrared spectroscopy.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04544669
Quelldatensatzuspto-grants-1985_10
ORD IDord-7ab17574bcec434eb7d00cc8a086cd2e
Quellennotizuspto-grants-1985_10