Reacción #1470425

ord-abc415fa4365433faddbdc5fd0cfe9e1

Ecuación de reacción

CC1(C)CC(OCC2CO2)CC(C)(C)N1O
1-oxyl-2,2,6,6-tetramethyl-4-glycidyloxypiperidine
OCCNCCO
diethanolamine
CC1(C)CC(OCC(O)CN(CCO)CCO)CC(C)(C)N1O
title compound
Rendimiento 29.9%
CC1(C)CC(OCC(O)CN(CCO)CCO)CC(C)(C)N1O
1-Oxyl-2,2,6,6-tetramethyl-4-{2-hydroxy-3-[di(2-hydroxyethyl)amino]propoxy}piperidine
Rendimiento 29.9%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ExtracciónThe solution is then extracted with methylene chloride
  2. 2
    ExtracciónThe methylene chloride extract
  3. 3
    Secadois dried over anhydrous magnesium sulfate
  4. 4
    Filtraciónfilter
  5. 5
    Concentraciónconcentrated
  6. 6
    OtroThe crude reaction product
  7. 7
    Otrois purified by column chromatography

Procedimiento

A solution of 2.28 g (0.01 mol) of 1-oxyl-2,2,6,6-tetramethyl-4-glycidyloxypiperidine and 1.05 g (0.01 mol) of diethanolamine in 25 mL of water is stirred at ambient temperature for 16 hours. The solution is then extracted with methylene chloride. The methylene chloride extract is dried over anhydrous magnesium sulfate, filter and concentrated. The crude reaction product is purified by column chromatography to afford 1.0 g of the title compound as a red oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06254724B1uspto-grants-2001_07