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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 66126Erstellt: 25. Oktober 2026

Phenethyl bromide → N-phenethyl-3-methoxyphenethylamine

https://huagongshe.com/reaction/66126

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenethyl bromideHCID 7666—
EduktAmmonium HydroxideHCID 14923—
Edukt3-MethoxyphenethylamineHCID 74866—
LösungsmittelWaterHCID 962—
ProduktN-phenethyl-3-methoxyphenethylamineHCID 1247799747,1%

Reaktionsbedingungen

Temperatur165 °C

Reaktionsschritte

A mixture of 1.51 g of β-(3-methoxyphenyl)-ethylamine and 1.85 g of β-phenethyl bromide was heated to 70°-80° C. on a bath and then was progressively heated to 165° C. over 10 minutes. The mixture was held at 165° C. for 5 minutes and was then cooled. 50 ml of water and then 4 ml of concentrated ammonium hydroxide were added thereto and the mixture was extracted 3 times with 40 ml of methylene chloride. The combined organic extracts were washed with 100 ml of aqueous sodium chloride solution and was dried over magnesium sulfate and was filtered. The filtrate was evaporated to dryness to obtain 3.4 g of raw product which was chromatographed over silica gel. Elution was with a 9-1 chloroform-ethanol mixture and the homogenous fraction with an Rf = 0.45 was taken to obtain 1.2 g of N-phenethyl-3-methoxyphenethylamine in the form of a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04130658
Quelldatensatzuspto-grants-1978_12
ORD IDord-2e873c5bc63843039c95682a71050375
Quellennotizuspto-grants-1978_12