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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1283972Erstellt: 25. Oktober 2026

Ethanol → N-benzyl-N-(3,4-dibenzyloxybenzoyl)methyl-2-(4-acetamidophenoxy)ethylamine

https://huagongshe.com/reaction/1283972

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium CarbonateHCID 10340—
Edukt3,4-Dibenzyloxyphenacyl bromideHCID 12681802—
EduktN-[2-(4-acetamidophenoxy)ethyl]benzylamineHCID 22750197—
LösungsmittelIsopropanolHCID 3776—
ProduktN-benzyl-N-(3,4-dibenzyloxybenzoyl)methyl-2-(4-acetamidophenoxy)ethylamineHCID 2275018166,9%

Reaktionsschritte

A mixture of 3,4-dibenzyloxyphenacyl bromide (32.8 g.), N-[2-(4-acetamidophenoxy)ethyl]benzylamine (22.8 g.), anhydrous sodium carbonate (8.4 g.) and ethanol (1 liter) was boiled under reflux for 2 hours, then filtered hot to remove the inorganic sediment and evaporated in vacuo to afford a thick syrup. The latter was dissolved in hot isopropanol and the solution cooled, the precipitated solid then being collected by filtration. To a hot solution of the solid in fresh isopropanol were added a few milliliters of ethyl acetate, and the solution was then allowed to cool to room temperature. The crystallized solid was collected by filtration, washed in diethyl ether and dried. Recrystallization from an isopropanol/ethyl acetate mixture afforded N-benzyl-N-(3,4-dibenzyloxybenzoyl)methyl-2-(4-acetamidophenoxy)ethylamine (32.8 g.), m.p. 104°-6°C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03976783
Quelldatensatzuspto-grants-1976_08
ORD IDord-740ae0bab8e74bfba8f48ec6ad15daaa
Quellennotizuspto-grants-1976_08