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Chloroacetonitrile → 3,4-Dimethoxyphenoxyacetonitrile

HRID 458792
ノート
印刷プレビュー

反応式

HRID 458792 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([OH:11])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].Cl[CH2:13][C:14]#[N:15].C([O-])([O-])=O.[K+].[K+].CCOC(C)=O.CCCCCC>CC(C)=O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:6]=[CH:7][C:8]=1[O:9][CH3:10])[O:11][CH2:13][C:14]#[N:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 7856ChloroacetonitrileHCID 11430Potassium CarbonateHCID 162513,4-DimethoxyphenolHCID 21226206Ethyl acetate hexane

生成物 1

HCID 189913533,4-Dimethoxyphenoxyacetonitrile収率 71.9%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

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

To a solution of 3,4-dimethoxyphenol (5.0 g, 32.4 mmol) in dry acetone (160 ml), were added chloroacetonitrile (2.05 ml, 32.4 mmol) and anhydrous K2CO3 (6.72 g, 48.6 mmol). The reaction mixture was stirred at reflux for 20 h under nitrogen. After cooling, the mixture was filtered and concentrated in vacuo. The residue was combined with H2O, extracted with CH2Cl2, and the combined organic phases were dried over anhydrous MgSO4, filtered and concentrated to give a crude oil. Flash chromatography (AcOEt/hexane: 3/7) gave the title product (4.5 g, 68%).

後処理

  1. temperatureat reflux for 20 h under nitrogen
  2. temperatureAfter cooling
  3. filtrationthe mixture was filtered
  4. concentrationconcentrated in vacuo
  5. extractionextracted with CH2Cl2
  6. dry with materialthe combined organic phases were dried over anhydrous MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customto give a crude oil

出典と根拠

ORDレコード
ord-8816e7b744094312af3b119e1ef6e794
出典データセット
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07192950B2

反応ノート

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