Potassium Cyanide → 2-(quinolin-2-yl)acetonitrile

HRID 1370502Notes

Reaction equation

HRID 1370502 reaction equation
Cl.Cl[CH2:3][C:4]1[CH:13]=[CH:12][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=1.C([O-])(O)=O.[Na+].[C-:19]#[N:20].[K+]>CCO.O>[N:5]1[C:6]2[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=2)[CH:12]=[CH:13][C:4]=1[CH2:3][C:19]#[N:20]

Participants

6

Reactant 3

HCID 9032Potassium CyanideHCID 516892Sodium BicarbonateHCID 30838232-(Chloromethyl)quinoline hydrochloride

Product 1

HCID 2643022-(quinolin-2-yl)acetonitrileYield 82%

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 962WaterSolvent

Procedure

To a suspension of 2-Chloromethyl-quinoline hydrochloride(TCI, 4.28 g, 20 mmol) in 50 mL of EtOH was added a solution of NaHCO3 (EM, 3.36 g, 40 mmol) in 30 mL of H2O. The mixture was stirred for 15 min, then was added KI (Aldrich, 4.5 g, 30 mmol) and KCN (Acros, 1.95 g, 30 mmol) and the resulting mixture was refluxed for 4h. after cooled to room temperature, EtOH was removed under reduced pressure. The residue was extracted 3× with EtOAc (200 mL). The organic layers were combined and washed twice with a brine solution (200 mL), dried over Na2SO4, and concentrated under vacuum. The residue was chromatographed (30% EtOAc/hexanes) to yield 2.76 g (82%) of product.

Workup

  1. temperaturethe resulting mixture was refluxed for 4h.
  2. customEtOH was removed under reduced pressure
  3. extractionThe residue was extracted 3× with EtOAc (200 mL)
  4. washwashed twice with a brine solution (200 mL)
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated under vacuum
  7. customThe residue was chromatographed (30% EtOAc/hexanes)

Sources & evidence

ORD record
ord-4b24819ec33145928ce150a9f06db124
Source dataset
uspto-grants-2003_06
Patent number
US06583157B2

Reaction notes

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