Pyridine → N-(2'-Diethylaminoethyl)phenoxyacetamide

HRID 26245

Reaktionsgleichung

Reaktionsgleichung von HRID 26245
[CH2:1]([N:3]([CH2:7][CH3:8])[CH2:4][CH2:5][NH2:6])[CH3:2].N1C=CC=CC=1.[O:15]([CH2:22][C:23](Cl)=[O:24])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C(Cl)Cl>[CH2:1]([N:3]([CH2:7][CH3:8])[CH2:4][CH2:5][NH:6][C:23](=[O:24])[CH2:22][O:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[CH3:2]

Komponenten

5

Edukt 3

HCID 1049PyridineHCID 60993N,N-DiethylethylenediamineHCID 69703Phenoxyacetyl chloride

Produkt 1

HCID 1563372N-(2'-Diethylaminoethyl)phenoxyacetamideAusbeute 66,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

First, 20 milliliters (0.05 mole) N,N-diethylethylene diamine, 50 milliliters methylene chloride, and 5.2 milliliters (0.065 mole) pyridine were combined in a flask. Next, 10.24 grams (0.06 mole) phenoxy acetyl chloride was added at -60° C. with stirring. The temperature was allowed to rise to 0° C. The reaction mixture was then washed with a 200 milliliter portion of water and a 100 milliliter portion of saturated sodium carbonate solution. The organic solution was stripped in vacuum to yield 8.3 grams of the desired product. nD30 1.5118.

Aufarbeitung

  1. customto rise to 0° C
  2. washThe reaction mixture was then washed with a 200 milliliter portion of water

Quellen und Nachweise

ORD-Eintrag
ord-327beb8f2bda47e7950c0217109a9ab4
Quelldatensatz
uspto-grants-1979_04
Patentnummer
US04148926

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