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m-Chloroperbenzoic acid → 2,4-dimethyl-3-chloromethylpyridine-N-oxide

HRID 1693
Notes
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Reaction equation

HRID 1693 reaction equation
[CH3:1][C:2]1[C:7]([CH2:8][Cl:9])=[C:6]([CH3:10])[CH:5]=[CH:4][N:3]=1.ClC1C=CC=C(C(OO)=[O:19])C=1>C(Cl)(Cl)Cl>[CH3:1][C:2]1[C:7]([CH2:8][Cl:9])=[C:6]([CH3:10])[CH:5]=[CH:4][N+:3]=1[O-:19]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 70297m-Chloroperbenzoic acidHCID 196909773-(Chloromethyl)-2,4-dimethylpyridine

Product 1

HCID 196909962,4-dimethyl-3-chloromethylpyridine-N-oxide

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent

Conditions

Temperature
0 °C

Procedure

The 2,4-dimethyl-3-chloromethylpyridine (21.5 g, 138 mmol) was dissolved in CHCl3 (800 mL) and cooled under nitrogen to 0° C. and m-chloroperbenzoic acid (55%, 35 g) was added in small portions. The reaction was stirred for 4 hours. The solution was extracted twice with saturated aqueous sodium bicarbonate (500 mL). The organic phase was dried with MgSO4, filtered and the solvent removed under reduced pressure. The residue was chromatographed on silica gel packed in 98:2 CH2 Cl2 :MeOH and eluted with same. The appropriate fractions were combined and the solvent was removed under reduced pressure the give the desired 2,4-dimethyl-3-chloromethylpyridine-N-oxide.

Workup

  1. extractionThe solution was extracted twice with saturated aqueous sodium bicarbonate (500 mL)
  2. dry with materialThe organic phase was dried with MgSO4
  3. filtrationfiltered
  4. customthe solvent removed under reduced pressure
  5. customThe residue was chromatographed on silica gel
  6. washMeOH and eluted with same
  7. customthe solvent was removed under reduced pressure the

Sources & evidence

ORD record
ord-bc2379efbe054eccaf35ae30843004da
Source dataset
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05726172

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes