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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 3,4-Dibenzyloxyphenacyl bromide | HCID 12681802 | — |
| Edukt | N-[2-(4-acetamidophenoxy)ethyl]benzylamine | HCID 22750197 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | N-benzyl-N-(3,4-dibenzyloxybenzoyl)methyl-2-(4-acetamidophenoxy)ethylamine | HCID 22750181 | 66,9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US03976783 |
|---|
| Quelldatensatz | uspto-grants-1976_08 |
|---|
| ORD ID | ord-740ae0bab8e74bfba8f48ec6ad15daaa |
|---|
| Quellennotiz | uspto-grants-1976_08 |
|---|