Reacción #470372

ord-fadb5e6e90674aed925a32b3cd7dbeec

Ecuación de reacción

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

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónfollowed by extraction
  2. 2
    LavadoThe organic layer was washed with 50 g of water ten times
  3. 3
    Otrodried

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08366956B2uspto-grants-2013_02