Acetic Acid → Acetic acid--1-ethyl-1H-imidazole (1/1)

HRID 20887

Reaction equation

HRID 20887 reaction equation
[C:1]([OH:4])(=[O:3])[CH3:2].[CH2:5]([N:7]1[CH:11]=[CH:10][N:9]=[CH:8]1)[CH3:6]>C(OCC)C>[C:1]([O-:4])(=[O:3])[CH3:2].[CH2:5]([N+:7]1[CH:11]=[CH:10][NH:9][CH:8]=1)[CH3:6]

Participants

4

Procedure

First, 6 ml of 99.7% acetic acid was added to 10 g of N-ethylimidazole, and the resultant mixture was stirred for 12 hours at a temperature kept at 0° C. The resultant reaction product was added dropwise to 1000 ml of diethyl ether under stirring. The diethyl ether was distilled off at room temperature, and the residue was dried under vacuum to precipitate crystals. The precipitated crystals were recovered to obtain 15.9 g of N-ethylimidazolium acetate. The product had a glass transition temperature of −51.7° C.

Workup

  1. customkept at 0° C
  2. customThe resultant reaction product
  3. distillationThe diethyl ether was distilled off at room temperature
  4. customthe residue was dried under vacuum
  5. customto precipitate crystals
  6. customThe precipitated crystals were recovered

Sources & evidence

ORD record
ord-26d8ff0da90a404e984d0ed38eb8c1ef
Source dataset
uspto-grants-2010_06
Patent number
US07746623B2

Linked notes

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