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Ethanol → 2-Cyano-2-methylpentanoic acid

HRID 358935
ノート
印刷プレビュー

反応式

HRID 358935 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 15099993HCID 15099993、化合物

生成物 1

HCID 147934792-Cyano-2-methylpentanoic acid収率 94.5%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-ec5f59235ae943c7b83c6dd6fdb578dc
出典データセット
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04999130

反応ノート

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