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Potassium Hydroxide → HCID 86627036, 화합물

HRID 2097482
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HRID 2097482 반응식
[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]
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참가 물질

4

반응물 2

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

생성물 1

HCID 86627036HCID 86627036, 화합물수율 100.2%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-036923b1d61a43e19986fa72c4f76be6
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08450319B2

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