Reaktion #470372

ord-fadb5e6e90674aed925a32b3cd7dbeec

Reaktionsgleichung

COC[N+]1(C)CCCC1.[Cl-]
N-methoxymethyl-N-methylpyrrolidinium chloride
COC[N+]1(C)CCCC1.[Cl-]
N-Methoxymethyl-N-Methylpyrrolidinium Chloride
O=S(=O)([N-]S(=O)(=O)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)F.[Li+]
lithium bis(pentafluoroethanesulfonyl)imide
ClCCl
dichloromethane
COC[N+]1(C)CCCC1.O=S(=O)([N-]S(=O)(=O)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)F
colorless liquid
COC[N+]1(C)CCCC1.O=S(=O)([N-]S(=O)(=O)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)F
N-Methoxymethyl-N-Methylpyrrolidinium bis(pentafluoroethanesulfonyl)imide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionfollowed by extraction
  2. 2
    WaschenThe organic layer was washed with 50 g of water ten times
  3. 3
    Sonstigedried

Vorschrift

A 15.0 g quantity of N-methoxymethyl-N-methylpyrrolidinium chloride prepared in Example 10 was dissolved in 50 g of water, and 35.1 g of lithium bis(pentafluoroethanesulfonyl)imide was added to the solution. The mixture was stirred for 30 minutes, and dichloromethane was thereafter added to the mixture, followed by extraction. The organic layer was washed with 50 g of water ten times and then dried, giving 31.4 g of a colorless liquid as the desired product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08366956B2uspto-grants-2013_02