m-Chloroperbenzoic acid → HCID 20095449, Verbindung

HRID 344805Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 344805
[C:1]([N:9]([CH3:19])[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([S:17][CH3:18])=[CH:13][CH:12]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.ClC1C=C(C=CC=1)C(OO)=[O:25]>ClCCl>[C:1]([N:9]([CH3:19])[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([S:17]([CH3:18])=[O:25])=[CH:13][CH:12]=1)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Komponenten

4

Versuchsvorschrift

To a solution of N-benzoyl-N-methyl-N-(4-methylthiobenzyl)amine (6.8 g) in dichloromethane (120 ml) is added gradually m-chloroperoxybenzoic acid (5.5 g) with stirring at a temperature below 5° C. and the mixture is stirred at the same temperature for 15 minutes. After the reaction, the reaction mixture is washed successively with 5% aqueous potassium carbonate solution and aqueous sodium chloride solution, and subsequently dried over magnesium sulfate. After dichloromethane is distilled off from the mixture, the residue is purified by silica gel column chromatography (solvent; dichloromethane:methanol=100:0-100:5) to give N-benzoyl-N-methyl-N-(4-methylsulfinylbenzyl)amine (4.1 g).

Aufarbeitung

  1. stirringthe mixture is stirred at the same temperature for 15 minutes
  2. customAfter the reaction
  3. washthe reaction mixture is washed successively with 5% aqueous potassium carbonate solution and aqueous sodium chloride solution
  4. dry with materialsubsequently dried over magnesium sulfate
  5. distillationAfter dichloromethane is distilled off from the mixture
  6. customthe residue is purified by silica gel column chromatography (solvent; dichloromethane:methanol=100:0-100:5)

Quellen und Nachweise

ORD-Eintrag
ord-6bc518fb476a491da1a36a1228655274
Quelldatensatz
uspto-grants-1991_10
Patentnummer
US05053514

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