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4-[3,5,6-Trimethyl-1,4-benzoquinon-2-yl(3-pyridyl)methyl]-alpha-methylcinnamic acid → 3-(4-[3,5,6-Trimethyl-1,4-benzoquinon-2-yl-(3-pyridyl)methyl]phenyl)propionic acid

HRID 484013
ノート
印刷プレビュー

反応式

HRID 484013 の反応式
[CH3:1][C:2]1[C:7](=[O:8])[C:6]([CH3:9])=[C:5]([CH3:10])[C:4](=[O:11])[C:3]=1[CH:12]([C:25]1[CH:26]=[N:27][CH:28]=[CH:29][CH:30]=1)[C:13]1[CH:24]=[CH:23][C:16]([CH:17]=[C:18](C)[C:19]([OH:21])=[O:20])=[CH:15][CH:14]=1>C(O)(=O)C.[Pd].[C]>[CH3:1][C:2]1[C:7](=[O:8])[C:6]([CH3:9])=[C:5]([CH3:10])[C:4](=[O:11])[C:3]=1[CH:12]([C:25]1[CH:26]=[N:27][CH:28]=[CH:29][CH:30]=1)[C:13]1[CH:24]=[CH:23][C:16]([CH2:17][CH2:18][C:19]([OH:21])=[O:20])=[CH:15][CH:14]=1
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 571128964-[3,5,6-Trimethyl-1,4-benzoquinon-2-yl(3-pyridyl)methyl]-alpha-methylcinnamic acid

生成物 1

HCID 142777693-(4-[3,5,6-Trimethyl-1,4-benzoquinon-2-yl-(3-pyridyl)methyl]phenyl)propionic acid収率 44.2%

試薬・触媒・溶媒 2

HCID 178418390HCID 178418390、化合物触媒HCID 176Acetic Acid溶媒

実験手順

4-[3,5,6-trimethyl-1,4-benzoquinon-2-yl-(3-pyridyl)methyl]-α-methylcinnamic acid, 0.7 g (1.75 mmol), was hydrogenated with 0.2 g of 5% Pd-carbon in 6 ml of acetic acid (the reaction completed in about 2 hours). The catalyst was filtered off, and the filtrate was concentrated, to which water was added and neutralized with a saturated aqueous solution of sodium hydrogen carbonate. The resultant substance was extracted with ethyl acetate, and oxidized by shaking with an aqueous solution of ferric chloride. After the organic phase was washed with water and dried, the solvent was evaporated off and the residue was purified with silica gel column chromatography (ethyl acetate-ethanol (9:1)) and recrystallized from ethyl acetate, to give 0.3 g (44.2%) of 3-(4-[3,5,6-trimethyl-1,4-benzoquinon-2-yl-(3-pyridyl)methyl]phenyl)propionic acid. The physical data are shown in Table 1.

後処理

  1. filtrationThe catalyst was filtered off
  2. concentrationthe filtrate was concentrated, to which water
  3. additionwas added
  4. extractionThe resultant substance was extracted with ethyl acetate
  5. washAfter the organic phase was washed with water
  6. customdried
  7. customthe solvent was evaporated off
  8. customthe residue was purified with silica gel column chromatography (ethyl acetate-ethanol (9:1))
  9. customrecrystallized from ethyl acetate

出典と根拠

ORDレコード
ord-b0456e628e0c4ca89bd748c0517d610c
出典データセット
uspto-grants-1993_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05229385

反応ノート

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