Diethyl Oxalate → 2,4-Dioxo-4-phenylbutanoic acid

HRID 68296

反応式

HRID 68296 の反応式
[C:1]([O:8]CC)(=[O:7])[C:2]([O:4]CC)=O.[O-]CC.[Na+].[C:15]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)(=[O:17])[CH3:16]>C(O)C>[O:4]=[C:2]([CH2:16][C:15](=[O:17])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C:1]([OH:8])=[O:7]

参加物

5

実験手順

To a stirred solution of diethyl oxalate (21.9 g, 150 mmol) and sodium ethoxide (168 mL, 21% wt. solution, 450 mmol) was added dropwise a solution of acetophenone (18 g, 150 mmol) in ethanol (120 mL). The reaction mixture was allowed to stir at ambient temperature for 15 h. The reaction mixture was concentrated to ca. 70 mL and partitioned between diethyl ether (50 mL) and water (200 mL). The phases were separated, and the aqueous layer adjusted to pH=1 with conc. HCl before being extracted with diethyl ether (3×100 mL). The combined ether extracts were dried over MgSO4 and evaporated to yield 2,4-dioxo-4-phenylbutanoic acid. 1H NMR (DMSO-d6, 300 MHz) δ 8.05 (d, J=7.2 Hz, 1.8H enol form), 7.96 (d, J=6.9 Hz, 0.2H keto form), 7.69 (t, J=7.5 Hz, 1H), 7.56 (t, J=8.1 Hz, 2H), 7.08 (s, 0.9H enol form), 4.56 (s, 0.1H keto form). 13C NMR (DMSO-d6, 75 MHz) δ 190.7, 170.7, 163.6, 135.1, 134.6, 129.7, 128.4, 98.5.

後処理

  1. concentrationThe reaction mixture was concentrated to ca. 70 mL
  2. custompartitioned between diethyl ether (50 mL) and water (200 mL)
  3. customThe phases were separated
  4. extractionbefore being extracted with diethyl ether (3×100 mL)
  5. dry with materialThe combined ether extracts were dried over MgSO4
  6. customevaporated

出典と根拠

ORDレコード
ord-af1398fb1f434988990d010148bcca00
出典データセット
uspto-grants-2014_09
特許番号
US08822451B2

関連ノート

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