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Potassium Carbonate → Ethyl 3-oxo-2-(propoxyimino)butanoate

HRID 543932
ノート
印刷プレビュー

反応式

HRID 543932 の反応式
[OH:1][N:2]=[C:3]([C:9](=[O:11])[CH3:10])[C:4]([O:6][CH2:7][CH3:8])=[O:5].C(=O)([O-])[O-].[K+].[K+].[CH2:18](I)[CH2:19][CH3:20]>CC(C)=O>[O:11]=[C:9]([CH3:10])[C:3](=[N:2][O:1][CH2:18][CH2:19][CH3:20])[C:4]([O:6][CH2:7][CH3:8])=[O:5]
参加物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 11430Potassium CarbonateHCID 336431-IodopropaneHCID 178472877HCID 178472877、化合物

生成物 1

HCID 54491732Ethyl 3-oxo-2-(propoxyimino)butanoate収率 81.2%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

To a suspension of ethyl 2-hydroxyimino-3-oxobutyrate (syn isomer, 15 g.) and potassium carbonate (19.8 g.) in acetone (75 ml.) was added dropwise propyliodide (16.2 g.) with stirring, and the mixture was stirred at ambient temperature for 1,5 hours. The insoluble substance was collected by filtration and washed with acetone. The washings and the filtrate were combined and evaporated to dryness under reduced pressure. To the resultant residue was added water and the aqueous solution was extracted twice with chloroform. The extract was washed with an aqueous solution of sodium chloride, dried over magnesium sulfate, and then evaporated to dryness under reduced pressure to give ethyl 3-oxo-2-propoxyiminobutyrate (syn isomer, 15.4 g.), oil.

後処理

  1. stirringthe mixture was stirred at ambient temperature for 1,5 hours
  2. filtrationThe insoluble substance was collected by filtration
  3. washwashed with acetone
  4. customevaporated to dryness under reduced pressure
  5. additionTo the resultant residue was added water
  6. extractionthe aqueous solution was extracted twice with chloroform
  7. washThe extract was washed with an aqueous solution of sodium chloride
  8. dry with materialdried over magnesium sulfate
  9. customevaporated to dryness under reduced pressure

出典と根拠

ORDレコード
ord-dff3c73d2c7241be9348832fa4846a7e
出典データセット
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04447430

反応ノート

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