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Dimethylformamide → 2-(Propan-2-yloxy)benzaldehyde

HRID 870492
ノート
印刷プレビュー

反応式

HRID 870492 の反応式
[OH:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].I[CH:11]([CH3:13])[CH3:12].C(=O)([O-])[O-].[K+].[K+].CN(C)C=O>>[CH3:12][CH:11]([O:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[O:5])[CH3:13]
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 4

HCID 6228DimethylformamideHCID 6362Isopropyl iodideHCID 6998SalicylaldehydeHCID 11430Potassium Carbonate

生成物 1

HCID 2500782-(Propan-2-yloxy)benzaldehyde収率 103.3%

実験手順

Into a 1000-mL 3-necked round-bottom flask was placed 2-hydroxybenzaldehyde (36 g, 294.79 mmol, 1.00 equiv), 2-iodopropane (100 g, 588.26 mmol, 2.00 equiv), potassium carbonate (122 g, 882.71 mmol, 2.99 equiv) and N,N-dimethylformamide (500 g, 6.84 mol, 23.21 equiv). The resulting solution was stirred overnight at room temperature. The reaction was then quenched by the addition of 1000 mL of water. The resulting solution was extracted with 3×500 mL of ethyl acetate and the organic layers combined, dried over anhydrous sodium sulfate and concentrated under vacuum to afford 50 g (crude) of 2-(propan-2-yloxy)benzaldehyde as a yellow oil.

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. customInto a 1000-mL 3-necked round-bottom flask was placed
  2. customThe reaction was then quenched by the addition of 1000 mL of water
  3. extractionThe resulting solution was extracted with 3×500 mL of ethyl acetate
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-4c36ea38a67946318a884aa183ca44fc
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08969557B2

反応ノート

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