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Water → 3-Formylbut-2-enyl acetate

HRID 21847
ノート
印刷プレビュー

反応式

HRID 21847 の反応式
[C:1]([O:4][CH2:5][CH:6]=[C:7]([CH3:10])[CH2:8][OH:9])(=[O:3])[CH3:2].O>CN(C)C=O>[C:1]([O:4][CH2:5][CH:6]=[C:7]([CH3:10])[CH:8]=[O:9])(=[O:3])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 962WaterHCID 5382224-Acetoxy-2-methyl-2-buten-1-ol

生成物 1

HCID 846993-Formylbut-2-enyl acetate収率 91.2%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a solution of 4-acetoxy-2-methyl-2-buten-1-ol (6.69 g, 46.4 mmol) in dimethylformamide (40 ml) were added 2,2,6,6-tetramethyl-piperidine-1-oxy (0.39 g, 2.32 mmol, 5 mol %) and cuprous chloride (0.48 g, 4.64 mmol, 10 mol %). The mixture was subjected to reaction for 8 hours while bubbling oxygen at a rate of about 100 ml/min. After completion of the reaction, the reaction mixture was poured into ice-cooled water (30 ml) and extracted with ether (100 ml) three times. The extract was dried over anhydrous magnesium sulfate. Evaporation of the ether followed by purification by column chromatography (ethyl acetate-hexane (=1:3)) gave 4-acetoxy-2-methyl-2-buten-1-al (6.02 g, 42.3 mmol; Yield: 91.2%).

後処理

  1. customThe mixture was subjected to reaction for 8 hours
  2. customwhile bubbling oxygen at a rate of about 100 ml/min
  3. customAfter completion of the reaction
  4. additionthe reaction mixture was poured into ice-
  5. extractionextracted with ether (100 ml) three times
  6. dry with materialThe extract was dried over anhydrous magnesium sulfate
  7. customEvaporation of the ether
  8. customfollowed by purification by column chromatography (ethyl acetate-hexane (=1:3))

出典と根拠

ORDレコード
ord-103d8784741446049982968a5a5bf106
出典データセット
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05424478

反応ノート

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