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Potassium Hydroxide → HCID 86627036、化合物

HRID 2097482
ノート
印刷プレビュー

反応式

HRID 2097482 の反応式
[CH2:1]([O:3][CH:4]([O:17][CH2:18][CH3:19])[CH2:5][CH:6]([C:12]([O:14]CC)=[O:13])[C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH3:2].[OH-].[K+:21]>C(O)C>[CH2:18]([O:17][CH:4]([O:3][CH2:1][CH3:2])[CH2:5][CH:6]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[C:12]([O-:14])=[O:13])[CH3:19].[K+:21]
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 2

HCID 14797Potassium HydroxideHCID 298328Diethyl 3,3-Diethoxypropane-1,1-dicarboxylate

生成物 1

HCID 86627036HCID 86627036、化合物収率 100.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To 15 L of dehydrated ethanol solution containing 2.48 Kg (purity: 95.1%., 8.54 mol) of diethyl 2-(2,2-diethoxyethyl)malonate was added 564 g (purity: 85%, 8.54 mol) of potassium hydroxide under argon gas atmosphere, and the mixture was stirred at room temperature for 4 hours. After completion of the reaction, the reaction mixture was concentrated under reduced pressure, 2 L of toluene was added to the obtained concentrate and the mixture was concentrated under reduced pressure. This operation of azeotropic dehydration with toluene was repeated three times to obtain 2.45 Kg of the title compound as a yellowish high-viscous oil substantially quantitatively.

後処理

  1. customAfter completion of the reaction
  2. concentrationthe reaction mixture was concentrated under reduced pressure, 2 L of toluene
  3. additionwas added to the obtained
  4. concentrationconcentrate
  5. concentrationthe mixture was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-036923b1d61a43e19986fa72c4f76be6
出典データセット
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08450319B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート