Reaktion #2045107

ord-9af0966e81364520a80f3acfd3ca9c8e

Reaktionsgleichung

O=C(Cl)C(Cl)(Cl)Cl
trichloroacetyl chloride
ClCCl
DCM
Cn1ccnc1
N-methylimidazole
ClCCl
DCM
Cn1cccc1C(=O)C(Cl)(Cl)Cl
product
Cn1cccc1C(=O)C(Cl)(Cl)Cl
1-Methyl-2-trichloroacetyl-1H-pyrrole

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenconcentrated
  2. 2
    Sonstigethe residue is purified over a flash frit (cyclohexane, cyclohexane/ethyl acetate 40:1)

Vorschrift

Under argon, 1.09 ml (12.3 mmol) of trichloroacetyl chloride are initially charged in 5 ml of DCM, and a solution of N-methylimidazole and 3 ml of DCM is added dropwise at RT over a period of 30 min. The reaction solution is allowed to stir at RT overnight and then concentrated, and the residue is purified over a flash frit (cyclohexane, cyclohexane/ethyl acetate 40:1). This gives the product as a liquid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08410090B2uspto-grants-2013_04