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

HRID 2396920ノート

反応式

HRID 2396920 の反応式
[CH3:1][O-].[Na+].[CH2:4]([O:6][C:7](=[O:17])[C:8]([CH2:15][CH3:16])(CC)P(O)(O)=O)C.[CH3:18]/[C:19](=C\CC)/[CH:20]=O.O>CO.O1CCCC1>[CH3:1]/[C:16](=[CH:18]\[CH2:19][CH3:20])/[CH:15]=[CH:8]/[C:7]([O:6][CH3:4])=[O:17]

参加物

7

反応物 4

HCID 962WaterHCID 5319754(E)-2-Methyl-2-pentenalHCID 10942334Sodium MethoxideHCID 17846631Ethyl diethyl-phosphonoacetate

生成物 1

HCID 12791883methyl (E,E)-4-methyl-2,4-heptadienoate

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a 28 wt % solution of sodium methoxide in methanol (226 g) at 20° C. was added dropwise diethyl phosphonoacetic acid ethyl ester (239.8 g). The solution was stirred at the same temperature for 30 minutes under a nitrogen atmosphere. A solution of (E)-2-methyl-2-pentenal (100 g) in tetrahydrofuran (200 ml) was added dropwise at 20° C. during 20 minutes and the solution was stirred for 1 hour. The reaction mixture was poured into chilled water and extracted twice with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo to give methyl (E,E)-4-methyl-2,4-heptadienoate (169.2 g) as an oil. This oil was used in the next reaction without further purification.

後処理

  1. stirringthe solution was stirred for 1 hour
  2. additionThe reaction mixture was poured
  3. extractionextracted twice with ethyl acetate
  4. washThe extract was washed with brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customevaporated in vacuo

出典と根拠

ORDレコード
ord-0d980af2ccb944e9a975fec44d0f1958
出典データセット
uspto-grants-1996_02
特許番号
US05495023

反応ノート

読み込み中…