Reaktion #1470425

ord-abc415fa4365433faddbdc5fd0cfe9e1

Reaktionsgleichung

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
Ausbeute 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
Ausbeute 29.9%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    ExtraktionThe solution is then extracted with methylene chloride
  2. 2
    ExtraktionThe methylene chloride extract
  3. 3
    Trocknenis dried over anhydrous magnesium sulfate
  4. 4
    Filtrationfilter
  5. 5
    Einengenconcentrated
  6. 6
    SonstigeThe crude reaction product
  7. 7
    Sonstigeis purified by column chromatography

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06254724B1uspto-grants-2001_07