m-Chloroperbenzoic acid → 2-Chloro-4-methylpyridine 1-oxide

HRID 631817

Reaktionsgleichung

Reaktionsgleichung von HRID 631817
[Cl:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N:3]=1.C1C=C(Cl)C=C(C(OO)=[O:17])C=1>C(Cl)Cl>[Cl:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N+:3]=1[O-:17]

Komponenten

4

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

2-Chloro-4-methylpyridine (1 g, 7.84 mmol) was dissolved in DCM (10 ml), cooled to 0° C., mCPBA (70%, 2.32 g, 9.41 mmol) was added and the mixture was stirred at 0° C. for several hours and allowed to reach room temperature overnight. The mixture was diluted with DCM and washed with saturated Na2S2O3 solution and saturated sodium bicarbonate solution. After drying (sodium sulfate) and concentration under reduced pressure, 1.0 g of a yellow oil was obtained (6.27 mmol, 80%) MS(ESI) m/z=144.0 [M+1]+.

Aufarbeitung

  1. washwashed with saturated Na2S2O3 solution and saturated sodium bicarbonate solution
  2. customAfter drying
  3. concentration(sodium sulfate) and concentration under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-8377b7d595bc4d13b1e0b8a8fc18f5b2
Quelldatensatz
uspto-grants-2016_04
Patentnummer
US09321724B2

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