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5-(2,3,4-Trimethoxyphenyl)-5-oxovaleric acid → 5-(2,3,4-Trimethoxyphenyl)pentanoic acid

HRID 33955
ノート
印刷プレビュー

反応式

HRID 33955 の反応式
O=[C:2]([C:9]1[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[C:11]([O:17][CH3:18])[C:10]=1[O:19][CH3:20])[CH2:3][CH2:4][CH2:5][C:6]([OH:8])=[O:7]>C(O)C.[Pd]>[CH3:20][O:19][C:10]1[C:11]([O:17][CH3:18])=[C:12]([O:15][CH3:16])[CH:13]=[CH:14][C:9]=1[CH2:2][CH2:3][CH2:4][CH2:5][C:6]([OH:8])=[O:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 193481585-(2,3,4-Trimethoxyphenyl)-5-oxovaleric acid

生成物 1

HCID 435890935-(2,3,4-Trimethoxyphenyl)pentanoic acid収率 97.74%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

5-Oxo-5-(2,3,4-trimethoxy-phenyl)-pentanoic acid (7.05 g 24.97 mmol) was dissolved in 100 mL of anhydrous ethanol under inert atmosphere and 2.0 g of Pd—C was added. The nitrogen gas was removed by vacuum, and hydrogen gas was passed into the flask. The reaction mixture was stirred for 1 h. The completion of the reaction was confirmed by TLC. The reaction mixture was filtered through celite. The solvent was evaporated under reduced pressure to obtain 6.48 g (97.74%) of 62 (colorless oil) which was pure by NMR.

後処理

  1. additionwas added
  2. customThe nitrogen gas was removed by vacuum, and hydrogen gas
  3. filtrationThe reaction mixture was filtered through celite
  4. customThe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-49a3d40815394918bb86530586be9444
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07429681B2

反応ノート

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