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Ethanol → 2-Cyano-2-methylpentanoic acid

HRID 358935
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HRID 358935 반응식
[C:1]([C:3]([CH3:12])([CH2:9][CH2:10][CH3:11])[C:4]([O:6]CC)=[O:5])#[N:2].C(O)C.[OH-].[Na+]>O>[C:1]([C:3]([CH3:12])([CH2:9][CH2:10][CH3:11])[C:4]([OH:6])=[O:5])#[N:2]
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참가 물질

5

반응물 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 15099993HCID 15099993, 화합물

생성물 1

HCID 147934792-Cyano-2-methylpentanoic acid수율 94.5%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

In a 200 ml two-necked round-bottom flask with ground fitting, 16.00 g (94.7 mM) of ethyl 2-cyano-2-methylpentanoate and 90 ml of ethanol were placed. To the mixture under stirring with a magnetic stirrer, a solution of 10.8 g (270 mM) of sodium hydroxide in 35 ml of distilled water was added dropwise. The mixture was stirred for 5 hours at room temperature, followed by removal of the solvent and addition of 3N-HCl until the solution reacted pH 1. The reaction mixture was transferred to a separating funnel, followed by three times of extraction with 50 ml of diethyl ether and washing with 50 ml of distilled water. The organic layer was dried on anhydrous sodium sulfate, followed by distilling-off of the solvent and reduced-pressure distillation to obtain 12.61 g (89.4 mM) of 2-cyano-2-methylpentanoic acid. Yield:94.4%, b.p.:120° C./2 mmHg.

후처리

  1. stirringThe mixture was stirred for 5 hours at room temperature
  2. customfollowed by removal of the solvent and addition of 3N-HCl until the solution
  3. customreacted pH 1
  4. customThe reaction mixture was transferred to a separating funnel
  5. extractionfollowed by three times of extraction with 50 ml of diethyl ether
  6. washwashing with 50 ml of distilled water
  7. dry with materialThe organic layer was dried on anhydrous sodium sulfate
  8. distillationfollowed by distilling-off of the solvent and reduced-pressure distillation

출처 및 근거

ORD 기록
ord-ec5f59235ae943c7b83c6dd6fdb578dc
출처 데이터셋
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04999130

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