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Ethyl 3-(dimethoxymethyl)-crotonate → Ethyl 3-methyl-4-oxobutanoate

HRID 1650775
ノート
印刷プレビュー

反応式

HRID 1650775 の反応式
C[O:2][CH:3](OC)/[C:4](/[CH3:11])=[CH:5]\[C:6]([O:8][CH2:9][CH3:10])=[O:7]>C(OCC)(=O)C.[Pd]>[CH:3]([CH:4]([CH3:11])[CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])=[O: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 1

HCID 13405211Ethyl 3-(dimethoxymethyl)-crotonate

生成物 1

HCID 13000833Ethyl 3-methyl-4-oxobutanoate収率 48%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 8857Ethyl Acetate溶媒

実験手順

A solution of ethyl 3-(dimethoxymethyl)-crotonate (73 g) in ethyl acetate (200 ml) was hydrogenated at 50 psi for 3 h in the presence of 10% palladium on charcoal (7 g). The solution was filtered, evaporated, and the residual oil treated with 0.25 M hydrogen chloride in 75% aqueous methanol for 2 h. To the reaction mixture was added ethyl acetate (300 ml) and water (150 ml). The organic phase was successively washed with sat. sodium bicarbonate solution (3×150 ml), water (100 ml) and dried over magnesium sulfate. The solution was concentrated in vacuo and the residual oil purified by chromatography on silica gel eluting with ethyl acetate-hexane (1:9) to give ethyl 3-formylbutyrate (26.5 g, 48%).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. filtrationThe solution was filtered
  2. customevaporated
  3. additionthe residual oil treated with 0.25 M hydrogen chloride in 75% aqueous methanol for 2 h
  4. additionTo the reaction mixture was added ethyl acetate (300 ml) and water (150 ml)
  5. washThe organic phase was successively washed with sat. sodium bicarbonate solution (3×150 ml), water (100 ml)
  6. dry with materialdried over magnesium sulfate
  7. concentrationThe solution was concentrated in vacuo
  8. customthe residual oil purified by chromatography on silica gel eluting with ethyl acetate-hexane (1:9)

出典と根拠

ORDレコード
ord-19a7fd19968544d489a087e687ecdcb8
出典データセット
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04925867

反応ノート

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