Ethanol → HCID 14793479, compound

HRID 358935Notes

Reaction equation

HRID 358935 reaction equation
[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]

Participants

5

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-ec5f59235ae943c7b83c6dd6fdb578dc
Source dataset
uspto-grants-1991_03
Patent number
US04999130

Reaction notes

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