Reaction #1460006

ord-80c4621d440c445d9f08a1c8efaa2dd9

Solvents

Conditions

Temperature
100°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherthe toluene removed
  2. 2
    Othera rotary evaporator
  3. 3
    Otherleaving a white solid residue that
  4. 4
    Otherwas triturated with toluene-hexane

Procedure

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)

Source

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