Ethanol → 2-Propenoic acid, 3-(4-chlorophenyl)-, ethyl ester

HRID 612939

反応式

HRID 612939 の反応式
[Cl:1][C:2]1[CH:12]=[CH:11][C:5]([CH:6]=[CH:7][C:8]([OH:10])=[O:9])=[CH:4][CH:3]=1.[CH2:13](O)[CH3:14].S(=O)(=O)(O)O>C1C=CC=CC=1>[CH2:13]([O:9][C:8](=[O:10])[CH:7]=[CH:6][C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:12][CH:11]=1)[CH3:14]

参加物

5

反応物 3

HCID 702EthanolHCID 1118Sulfuric AcidHCID 153712-Propenoic acid, 3-(4-chlorophenyl)-

生成物 1

HCID 2014712-Propenoic acid, 3-(4-chlorophenyl)-, ethyl ester収率 97%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

4-Chlorocinnamic acid (300 g) was suspended in benzene (1200 ml), and ethanol (340 g) and conc. sulfuric acid (14 ml) were added thereto, followed by reflux of the resulting mixture for 15 hours. After the reaction mixture had been washed successively with a diluted aqueous NaCl solution (500 ml), a saturated aqueous sodium hydrogencarbonate solution (500 ml) and a dilute aqueous NaCl solution (500 ml), the organic layer was dried over anhydrous magnesium sulfate. After filtration, the solvent was evaporated under reduced pressure. The residue was evaporated under reduced pressure to obtain the title compound (334 g, 97%) as a colorless liquid.

後処理

  1. temperatureby reflux of the resulting mixture for 15 hours
  2. washAfter the reaction mixture had been washed successively with a diluted aqueous NaCl solution (500 ml)
  3. dry with materiala saturated aqueous sodium hydrogencarbonate solution (500 ml) and a dilute aqueous NaCl solution (500 ml), the organic layer was dried over anhydrous magnesium sulfate
  4. filtrationAfter filtration
  5. customthe solvent was evaporated under reduced pressure
  6. customThe residue was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-a941244f89f74b54958785deed1f5d32
出典データセット
uspto-grants-1999_12
特許番号
US06005116

関連ノート

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