Reacción #1194

ord-ad4349523f614af097d0bd73d457fcbf

Ecuación de reacción

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

Disolventes

Condiciones de reacción

Temperatura
80°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroA 200-ml two-necked flask equipped with a stirrer
  2. 2
    Temperaturareflux tube
  3. 3
    TemperaturaWhile heating
  4. 4
    workup.STIRRINGstirred further for 18 hours
  5. 5
    Concentraciónit was concentrated under reduced pressure
  6. 6
    Otrothe resultant residue was purified by column chromatography on silica gel

Procedimiento

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).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723497uspto-grants-1998_03