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3-(4-ethylphenyl)prop-2-enoic Acid → 3-(4-ethylphenyl)propanoic Acid

HRID 1956166
ノート
印刷プレビュー

反応式

HRID 1956166 の反応式
[CH2:1]([C:3]1[CH:13]=[CH:12][C:6]([CH:7]=[CH:8][C:9]([OH:11])=[O:10])=[CH:5][CH:4]=1)[CH3:2]>C(O)(=O)C.[Pd]>[CH2:1]([C:3]1[CH:13]=[CH:12][C:6]([CH2:7][CH2:8][C:9]([OH:11])=[O:10])=[CH:5][CH:4]=1)[CH3:2]
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 14827523-(4-ethylphenyl)prop-2-enoic Acid

生成物 1

HCID 20640393-(4-ethylphenyl)propanoic Acid

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 176Acetic Acid溶媒

実験手順

A solution containing 18 g of 4-ethylcinnamic acid dissolved in 50 mL of acetic acid was placed in a Parr Shaker bomb flask, 1.0 g of 5% palladium on carbon catalyst was added, and the flask was pressured to 50 psig (pounds per square inch gauge) (4460 kiloPascals) for 2 hours. The catalyst was then removed by filtration and the solution was concentrated by evaporation under reduced pressure. Water was added to the residue and the solid present was collected by filtration and dried under reduced pressure to obtain 3-(4-ethylphenyl)propanoic acid.

後処理

  1. additionwas added
  2. customThe catalyst was then removed by filtration
  3. concentrationthe solution was concentrated by evaporation under reduced pressure
  4. additionWater was added to the residue
  5. filtrationthe solid present was collected by filtration
  6. customdried under reduced pressure

出典と根拠

ORDレコード
ord-ca95abd84ef341a7997ba843f063a757
出典データセット
uspto-grants-1998_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05780465

反応ノート

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