Reaktion #1194

ord-ad4349523f614af097d0bd73d457fcbf

Reaktionsgleichung

NCCO
ethanolamine
CCCCC(CC)COCCCCCCCCCCOCC1CO1
10-(2-ethylhexyloxy)decyl glycidyl ether
CCCCC(CC)COCCCCCCCCCCOCC(O)CNCCO
title compound
Ausbeute 68.4%
CCCCC(CC)COCCCCCCCCCCOCC(O)CNCCO
1-(2-hydroxyethylamino)-3-[10-(2-ethylhexyloxy)decyloxy]-2-propanol
Ausbeute 68.4%

Lösungsmittel

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA 200-ml two-necked flask equipped with a stirrer
  2. 2
    Temperaturreflux tube
  3. 3
    TemperaturWhile heating
  4. 4
    workup.STIRRINGstirred further for 18 hours
  5. 5
    Einengenit was concentrated under reduced pressure
  6. 6
    Sonstigethe resultant residue was purified by column chromatography on silica gel

Vorschrift

A 200-ml two-necked flask equipped with a stirrer, reflux tube and dropping funnel was charged with 32.7 g (0.54 mol) of ethanolamine and 10.1 g of ethanol. While heating and stirring the mixture at 80° C., 1.76 g (5.14 mmol) of 10-(2-ethylhexyloxy)decyl glycidyl ether were added dropwise over 2 hours. After the resultant mixture was heated and stirred further for 18 hours, it was concentrated under reduced pressure, and the resultant residue was purified by column chromatography on silica gel, thereby obtaining 1.42 g (yield: 68%) of the title compound (Ia-14).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723497uspto-grants-1998_03