m-Chloroperbenzoic acid → 2-Chloromethyl-3-methylpyridine 1-oxide

HRID 35448Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 35448
[Cl:1][CH2:2][C:3]1[C:8]([CH3:9])=[CH:7][CH:6]=[CH:5][N:4]=1.ClC1C=CC=C(C(OO)=[O:18])C=1>C(Cl)Cl>[Cl:1][CH2:2][C:3]1[C:8]([CH3:9])=[CH:7][CH:6]=[CH:5][N+:4]=1[O-:18]

Komponenten

4

Edukt 2

HCID 70297m-Chloroperbenzoic acidHCID 130586822-(Chloromethyl)-3-methylpyridine

Produkt 1

HCID 221514452-Chloromethyl-3-methylpyridine 1-oxide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

A solution of 24 g (0.17 mol) of 2-chloromethyl-3-methylpyridine in 200 ml of methylene chloride ls treated while cooling with ice with a solution of 44 g (0.25 mol) of m-chloroperbenzoic acid in 200 ml of methylene chloride. The reaction mixture is heated under reflux for 2 hours and concentrated in a rotary evaporator. The residue is chromatographed on silica gel with ethyl acetate/methylene chloride (3:1) as the elution agent, the medium pressure flash chromatography method being used and the pressure being produced with nitrogen gas. The 2-chloromethyl-3-methyl-pyridine 1-oxide obtained is processed directly.

Aufarbeitung

  1. temperatureThe reaction mixture is heated
  2. temperatureunder reflux for 2 hours
  3. concentrationconcentrated in a rotary evaporator
  4. customThe residue is chromatographed on silica gel with ethyl acetate/methylene chloride (3:1) as the elution agent
  5. customthe pressure being produced with nitrogen gas

Quellen und Nachweise

ORD-Eintrag
ord-516fd9b40dca499c90a5cb950e6cde5d
Quelldatensatz
uspto-grants-1988_08
Patentnummer
US04766133

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