Reaktion #1460006

ord-80c4621d440c445d9f08a1c8efaa2dd9

Reaktionsgleichung

CN(CC(O)CN(C)S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
[C4F9SO2N(CH3)CH2]2CHOH
O=C1CCC(=O)O1
succinic anhydride
CN(CC(CN(C)S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)OC(=O)CCC(=O)O)S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
[C4F9SO2N(CH3)CH2]2CHOC(O)C2H4COOH
Ausbeute 66.5%

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe toluene removed
  2. 2
    Sonstigea rotary evaporator
  3. 3
    Sonstigeleaving a white solid residue that
  4. 4
    Sonstigewas triturated with toluene-hexane

Vorschrift

A 250 mL three necked round bottom was charged with [C4F9SO2N(CH3)CH2]2CHOH (6.8 g; 10 mmole), succinic anhydride 1.0 g; 10 mmole) 4-dimethylaminopyridine (0.1 g) and toluene (100 mL). The ensuing mixture was stirred at 100° C. overnight, the toluene removed using a rotary evaporator, leaving a white solid residue that was triturated with toluene-hexane to yield [C4F9SO2N(CH3)CH2]2CHOC(O)C2H4COOH (5.2 g)

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07160850B2uspto-grants-2007_01