Diethyl Malonate → Ethyl 2-Ethoxycarbonyl-4-(4-octylphenyl)butyrate

HRID 862852ノート

反応式

HRID 862852 の反応式
[Na].[C:2]([O:10][CH2:11][CH3:12])(=[O:9])[CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].[CH2:13]([C:21]1[CH:26]=[CH:25][C:24]([CH2:27][CH2:28]I)=[CH:23][CH:22]=1)[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]>C(O)C>[CH2:11]([O:10][C:2]([CH:3]([CH2:28][CH2:27][C:24]1[CH:23]=[CH:22][C:21]([CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])=[CH:26][CH:25]=1)[C:4]([O:6][CH2:7][CH3:8])=[O:5])=[O:9])[CH3:12]

参加物

5

反応物 3

HCID 7761Diethyl MalonateHCID 5360545SodiumHCID 105453621-(2-Iodoethyl)-4-octylbenzene

生成物 1

HCID 21849265Ethyl 2-Ethoxycarbonyl-4-(4-octylphenyl)butyrate収率 65.9%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
40 °C

実験手順

Sodium (2.67 g) was dissolved in absolute ethanol (100 ml) and diethyl malonate (18.6 g) was dropwise added thereto at 27°-30° C. for 3 minutes. The mixture was stirred at 40° C. for 40 minutes and 2-(4-octylphenyl)ethyl iodide (40 g) was dropwise added to the reaction mixture at 44°-45° C. over 10 minutes. The mixture was refluxed at 50° C. for 1 hour and stirred under heating for 1.5 hours. The reaction mixture was cooled and the solvent was distilled away under reduced pressure. Water was added thereto and extracted with ethyl acetate. The extract was washed with water and dried over magnesium sulfate. The solvent was distilled away under reduced pressure and the residue obtained was subjected to silica gel column chromatography to give the subject compound (28.8 g).

後処理

  1. temperatureThe mixture was refluxed at 50° C. for 1 hour
  2. stirringstirred
  3. temperatureunder heating for 1.5 hours
  4. temperatureThe reaction mixture was cooled
  5. distillationthe solvent was distilled away under reduced pressure
  6. additionWater was added
  7. extractionextracted with ethyl acetate
  8. washThe extract was washed with water
  9. dry with materialdried over magnesium sulfate
  10. distillationThe solvent was distilled away under reduced pressure
  11. customthe residue obtained

出典と根拠

ORDレコード
ord-2489e87f634d4ae2b077fa42029f6f01
出典データセット
uspto-grants-1998_02
特許番号
US05719176

反応ノート

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