m-Chloroperbenzoic acid → 2-(4-methylphenyl)-6-methylpyridine-N-oxide

HRID 1077839

反応式

HRID 1077839 の反応式
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([CH3:14])[N:9]=2)=[CH:4][CH:3]=1.ClC1C=CC=C(C(OO)=[O:23])C=1>C(Cl)(Cl)Cl>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([CH3:14])[N+:9]=2[O-:23])=[CH:6][CH:7]=1

参加物

4

反応物 2

HCID 70297m-Chloroperbenzoic acidHCID 6030812-Methyl-6-(4-methylphenyl)pyridine

生成物 1

HCID 194303302-(4-methylphenyl)-6-methylpyridine-N-oxide収率 57.2%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒2 回

実験手順

A solution of 2-(4-methylphenyl)-6-methylpyridine (4.5 g) in 100 ml of chloroform was cooled to 0° C., and m-chloroperbenzoic acid (7.7 g) in 50 ml of chloroform was added over a period of 15 minutes. The mixture was stirred at room temperature for 3 hours, then at 50° C. for 2 hours, followed by stirring overnight at room temperature. Solvent was evaporated to a small volume under reduced pressure, and the residue passed through an alumina column, eluting with 2% methanol in methylene chloride to remove benzoic acid. The eluate was flash-chromatographed on silica gel, eluting with 5% methanol in methylene chloride, to yield 2.8 g of 2-(4-methylphenyl)-6-methylpyridine-N-oxide, m.p. 95° C.

後処理

  1. waitat 50° C. for 2 hours
  2. stirringby stirring overnight at room temperature
  3. customSolvent was evaporated to a small volume under reduced pressure
  4. washeluting with 2% methanol in methylene chloride
  5. customto remove benzoic acid
  6. customThe eluate was flash-chromatographed on silica gel
  7. washeluting with 5% methanol in methylene chloride

出典と根拠

ORDレコード
ord-6666939eed814061b84f82f13e26e1cd
出典データセット
uspto-grants-1996_08
特許番号
US05545645

関連ノート

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