Diethyl methylmalonate → Diethyl 2-methyl-2-(4-pyridylmethyl)malonate

HRID 18386

反応式

HRID 18386 の反応式
[H-].[Na+].[CH3:3][CH:4]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[C:5]([O:7][CH2:8][CH3:9])=[O:6].Cl[C:16]1[CH:21]=[CH:20][N:19]=[C:18](CCl)[CH:17]=1.[C:24](=O)([O-])O.[Na+]>CN(C)C=O>[CH3:3][C:4]([CH2:24][C:16]1[CH:17]=[CH:18][N:19]=[CH:20][CH:21]=1)([C:5]([O:7][CH2:8][CH3:9])=[O:6])[C:10]([O:12][CH2:13][CH3:14])=[O:11]

参加物

6

実験手順

N,N-Dimethylformamide (143 ml) was added to sodium hydride (5.36 g, 134 mmol) under a nitrogen atmosphere, and the mixture was stirred under ice-cooling. A solution of diethyl methylmalonate (11.7 g, 67.1 mmol) in N,N-dimethylformamide (40 ml) was added dropwise to the mixture over five minutes, after 10 minutes, 4-chloropicolyl hydrochloride (10.0 g, 61.0 mmol) was added thereto little by little over five minutes, and the temperature was raised to room temperature. After one hour, a saturated aqueous sodium hydrogencarbonate solution (500 ml) was added to the reaction mixture, and the whole was extracted with diethyl ether (400 ml). The organic layer was washed with water (100 ml) and saturated brine (50 ml) successively, dried over magnesium sulfate and concentrated under reduced pressure to give diethyl 2-methyl-2-(4-pyridylmethyl)malonate (17.2 g, quantitatively, containing sodium hydride oil) as a brown oily matter.

後処理

  1. temperaturecooling
  2. waitAfter one hour
  3. extractionthe whole was extracted with diethyl ether (400 ml)
  4. washThe organic layer was washed with water (100 ml) and saturated brine (50 ml) successively
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-6432125f3aa84159a01537069af106c9
出典データセット
uspto-grants-2010_06
特許番号
US07741346B2

関連ノート

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