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Hydrogen Peroxide → 3,4-Dimethylpyridine 1-oxide

HRID 236450
ノート
印刷プレビュー

反応式

HRID 236450 の反応式
[N:1]1[CH:6]=[CH:5][C:4]([CH3:7])=[C:3]([CH3:8])[CH:2]=1.[OH:9]O.CCCCCC>C(O)(=O)C>[N+:1]1([O-:9])[CH:6]=[CH:5][C:4]([CH3:7])=[C:3]([CH3:8])[CH:2]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 784Hydrogen Peroxide3 回HCID 8058HexaneHCID 114173,4-Dimethylpyridine

生成物 1

HCID 3024543,4-Dimethylpyridine 1-oxide収率 83%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
75 °C

実験手順

The general procedure of Boekelheide1 for the preparation of hydroxymethylpyridines was used. Thus, a solution of freshly distilled 3,4-lutidine (46.0 g, 0.43 mol) in 120 mL of glacial acetic acid was cooled at 0° C. and then 64 mL of 30% H2O2 was added dropwise. The resulting solution was heated at 75° C. (oil-bath temperature) for 3 h. Another 20 mL of 30% H2O2 was then added and heating was continued for 18 h. Finally, 20 mL of 30% H2O2 was again added and the reaction was kept at 75° C. for another 3 h. The solution was then concentrated to about 100 mL under water-aspirator pressure, 50 mL of H2O was added and the mixture was concentrated to about one half volume. The resulting mixture was cooled (0°-5° C.) and basified to about pH 10 using cold 40% aqeuous NaOH. The mixture was then extracted with CH2Cl2 (5×) and the extract was dried (Na2CO3 +Na2SO4) and concentrated on the roto-vap to give a yellow solution. Dilution of this solution with hexane afforded a solid which was collected by filtration and then dried in vacuo to give 3,4-lutidine-N-oxide (48.0 g, 83%) as an off-white solid.

後処理

  1. temperatureheating
  2. waitthe reaction was kept at 75° C. for another 3 h
  3. concentrationThe solution was then concentrated to about 100 mL under water-aspirator pressure, 50 mL of H2O
  4. additionwas added
  5. concentrationthe mixture was concentrated to about one half volume
  6. temperatureThe resulting mixture was cooled (0°-5° C.)
  7. extractionThe mixture was then extracted with CH2Cl2 (5×)
  8. dry with materialthe extract was dried (Na2CO3 +Na2SO4)
  9. concentrationconcentrated on the roto-vap
  10. customto give a yellow solution
  11. filtrationwas collected by filtration
  12. customdried in vacuo

出典と根拠

ORDレコード
ord-4af8f3a4bb8a4f39aebfdcb5551bc651
出典データセット
uspto-grants-1987_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04644061

反応ノート

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