Potassium Iodide → 1-(6-Chlorobenzotriazol-1-yl)-propan-2-one

HRID 7216

Reaktionsgleichung

Reaktionsgleichung von HRID 7216
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]2[NH:6][N:7]=[N:8][C:4]=2[CH:3]=1.Cl[CH2:12][C:13](=[O:15])[CH3:14].C(=O)([O-])[O-].[K+].[K+].[I-].[K+]>CC(C)=O>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]2[N:6]([CH2:12][C:13](=[O:15])[CH3:14])[N:7]=[N:8][C:4]=2[CH:3]=1.[Cl:1][C:2]1[CH:10]=[CH:9][C:5]2[N:6]=[N:7][N:8]([CH2:12][C:13](=[O:15])[CH3:14])[C:4]=2[CH:3]=1

Komponenten

7

Versuchsvorschrift

A mixture of 5 g of 5-chlorobenzotriazole, 1.4 g of chloroacetone, 5.1 g of potassium carbonate and 0.5 g of potassium iodide is stirred into 50 ml of acetone at room temperature for 48 h. The mixture is subsequently filtered, the filtrate concentrated by evaporation in a vacuum, and the residue purified by flash chromatography. In this way, two isomeric products, 1-(5-chlorobenzotriazol-1-yl)-propan-2-one and 1-(6-chlorobenzotriazol-1-yl)-propan-2-one, are isolated in approximately the same quantities, the first of which is then used directly in the next step.

Aufarbeitung

  1. filtrationThe mixture is subsequently filtered
  2. concentrationthe filtrate concentrated by evaporation in a vacuum
  3. customthe residue purified by flash chromatography

Quellen und Nachweise

ORD-Eintrag
ord-1afeb603539e4cb68b366cc59118d27f
Quelldatensatz
uspto-grants-2006_08
Patentnummer
US07084280B2

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