Sodium Hydroxide → 3-Methyl-5-phenyl-2,4-pentadienoic acid

HRID 601071

反応式

HRID 601071 の反応式
[CH3:1][C:2]([CH:6]=[CH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=[CH:3][CH:4]=[O:5].[OH-:14].[Na+]>C(O)C.O.[N+]([O-])([O-])=O.[Ag+]>[CH3:1][C:2]([CH:6]=[CH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=[CH:3][C:4]([OH:14])=[O:5]

参加物

6

実験手順

To a stirred solution of 3-methyl-5-phenyl-2,4-pentadienal (16.5 g) in ethanol (330 mL) was added dropwise a solution of silver nitrate (19.28 g) in water (160 mL) followed by dropwise addition of an aqueous sodium hydroxide (25 g, 80 mL) solution. The resulting mixture was allowed to stir for an additional five hours and then filtered. The solid was washed with ethanol. The combined filtrate was concentrated in vacuum. The residue was dissolved in water (200 mL). The aqueous solution was extracted with ether (300 mL) twice and acidified with 6 N hydrochloric acid (74 mL). The solid formed was filtered and recrystallized from methanol (40 mL) to yield 2.65 g of the desired 3-methyl-5-phenyl-2,4-pentadienoic acid. 1H NMR (acetone-d6, 300 MHz), δ (ppm) 7.60 (d, 2H), 7.35 (m, 3H), 7.06 (m, 2H), 6.02 (broad s, 1H), 2.50 (s, 3H).

後処理

  1. filtrationfiltered
  2. washThe solid was washed with ethanol
  3. concentrationThe combined filtrate was concentrated in vacuum
  4. dissolutionThe residue was dissolved in water (200 mL)
  5. extractionThe aqueous solution was extracted with ether (300 mL) twice
  6. customThe solid formed
  7. filtrationwas filtered
  8. customrecrystallized from methanol (40 mL)

出典と根拠

ORDレコード
ord-00e702d7447341e79c5f76a16f4d3742
出典データセット
uspto-grants-2011_03
特許番号
US07902259B2

関連ノート

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