Reacción #1211

ord-f7c05078e24046a8887d238bff8b0c4f

Ecuación de reacción

[K+].[OH-]
KOH
N#N
N2
O=C(CCCCCCCCCCCCCCCO)N(CCO)CCO
N,N-bis(2-hydroxyethyl)-16-hydroxyhexadecanamide
[Al+3].[H-].[H-].[H-].[H-].[Li+]
LiAlH4
OCCCCCCCCCCCCCCCCN(CCO)CCO
title compound
Rendimiento 62.0%
OCCCCCCCCCCCCCCCCN(CCO)CCO
16-[N,N-bis(2-hydroxyethyl)amino]-1-hexadecanol
Rendimiento 62.0%

Disolventes

Condiciones de reacción

Temperatura
65°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroA 500-ml flask equipped with a stirrer
  2. 2
    Temperaturareflux condenser
  3. 3
    workup.ADDITIONwere added
  4. 4
    TemperaturaAfter cooling the reaction mixture to room temperature
  5. 5
    Otroa salt deposited was separated by filtration
  6. 6
    workup.DISTILLATIONThe solvent was then distilled off under reduced pressure
  7. 7
    Otrothe resultant residue was purified by column chromatography on silica gel

Procedimiento

A 500-ml flask equipped with a stirrer and reflux condenser was charged with 3.01 g (79.3 mmol) of LiAlH4 and 200 ml of tetrahydrofuran. While stirring the mixture at room temperature in an N2 atmosphere, 5.00 g (13.9 mmol) of N,N-bis(2-hydroxyethyl)-16-hydroxyhexadecanamide were added, followed by stirring at 65° C. for 18 hours. After cooling the reaction mixture to room temperature, 15 g of 3% aqueous KOH were added, and a salt deposited was separated by filtration. The solvent was then distilled off under reduced pressure, and the resultant residue was purified by column chromatography on silica gel, thereby obtaining 2.98 g (yield: 62%) of the title compound (IId-3).

Fuente

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