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Sodium Chloride → 159017-89-7

HRID 1828253
ノート
印刷プレビュー

反応式

HRID 1828253 の反応式
[CH:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([CH:11](O)[CH3:12])=[CH:7][CH:6]=1)([CH3:3])[CH3:2].P(Cl)(Cl)(Cl)=O.[Cl-].[Na+].CN(C)[CH:23]=[O:24]>>[CH:1]([O:4][C:5]1[CH:10]=[CH:9][C:8](/[CH:11]=[CH:12]/[CH:23]=[O:24])=[CH:7][CH:6]=1)([CH3:3])[CH3:2]
参加物反応条件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 5234Sodium ChlorideHCID 6228Dimethylformamide2 回HCID 24813Phosphorus oxychlorideHCID 11148076HCID 11148076、化合物

生成物 1

HCID 11805523159017-89-7

反応条件

温度
0 °C

実験手順

A solution of 1-(4-isopropyloxy phenyl) ethanol of formula 4 (4.8 g, 27 mmol) in dimethyl formamide (10 ml) is slowly added to phosphorus oxychloride (8 ml) in DMF (12 ml) with stirring at 0° C. The reaction mixture is stirred for 2 hours then allowed attaining room temperature followed by heating on an oil bath for 36 hour at 40° C. After the completion of the reaction as monitored by TLC, contents of the reaction mixture are poured into ice cold water (500 ml), neutralised with dilute alkali solution and saturated by adding sodium chloride. The aqueous portion is extracted with ethyl acetate (3×100 ml), organic layer washed with water, dried over anhydrous sodium sulphate and stripped off the solvent under vacuum to furnish crude product (4.8 g). It was purified by column chromatography over silica gel to yield a semisolid 3-(4-isopropyloxy phenyl)-2E-propenal of formula 3 (80%).

後処理

  1. stirringThe reaction mixture is stirred for 2 hours
  2. customthen allowed attaining room temperature
  3. temperatureby heating on an oil bath for 36 hour at 40° C
  4. customAfter the completion of the reaction
  5. additionwith dilute alkali solution
  6. extractionThe aqueous portion is extracted with ethyl acetate (3×100 ml), organic layer
  7. washwashed with water
  8. dry with materialdried over anhydrous sodium sulphate
  9. customto furnish crude product (4.8 g)
  10. customIt was purified by column chromatography over silica gel

出典と根拠

ORDレコード
ord-96a3bb66c92242fd976f5779e45a7b67
出典データセット
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07057040B2

反応ノート

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