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Water → methyl (E,E)-4-ethyl-2,4-heptadienoate

HRID 2295014
ノート
印刷プレビュー

反応式

HRID 2295014 の反応式
C[O-].[Na+].[CH2:4]([O:6][C:7](=[O:17])[C:8](CC)(CC)P(O)(O)=O)C.[CH2:18](/[C:20](=[CH:23]\[CH2:24][CH3:25])/[CH:21]=O)[CH3:19].O>CO>[CH2:18](/[C:20](=[CH:23]\[CH2:24][CH3:25])/[CH:21]=[CH:8]/[C:7]([O:6][CH3:4])=[O:17])[CH3:19]
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 962WaterHCID 53644392-Pentenal, 2-ethyl-HCID 10942334Sodium MethoxideHCID 17846631Ethyl diethyl-phosphonoacetate

生成物 1

HCID 12700325methyl (E,E)-4-ethyl-2,4-heptadienoate収率 77.7%

試薬・触媒・溶媒 1

HCID 887Methanol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 28 wt % solution of sodium methoxide in methanol (25.7 g) at 10° C. were added dropwise diethyl phosphonoacetic acid ethyl ester (25.3 g) and (E)-2-ethyl-2-pentenal (11.5 g) successively under a nitrogen atmosphere. The reaction mixture was stirred at room temperature for 3 hours, poured into chilled water and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel (dichloromethane) to give 13.4 g of methyl (E,E)-4-ethyl-2,4-heptadienoate as an oil.

後処理

  1. additionpoured
  2. extractionextracted with ethyl acetate
  3. washThe extract was washed with brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customevaporated in vacuo
  6. customThe residue was chromatographed on silica gel (dichloromethane)

出典と根拠

ORDレコード
ord-42ceaf244aec4e628be00ff2ba7ddf13
出典データセット
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05691366

反応ノート

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