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Sodium Cyanide → (1-Pyridin-2-yl-cyclopentyl)-acetonitrile

HRID 2169464
Notes
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Reaction equation

HRID 2169464 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1([CH2:12]OS(C)(=O)=O)[CH2:11][CH2:10][CH2:9][CH2:8]1.[C-:18]#[N:19].[Na+]>CS(C)=O>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1([CH2:12][C:18]#[N:19])[CH2:11][CH2:10][CH2:9][CH2:8]1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 8929Sodium CyanideHCID 86726091Methanesulfonic acid 1-pyridin-2-yl-cyclopentylmethyl ester

Product 1

HCID 86726092(1-Pyridin-2-yl-cyclopentyl)-acetonitrileYield 82.1%

Reagents, catalysts & solvents 1

HCID 679Dimethyl SulfoxideSolvent

Conditions

Temperature
140 °C

Procedure

To a stirred solution of methanesulfonic acid 1-pyridin-2-yl-cyclopentylmethyl ester (433) (2 g, 7.843 mmol) in dimethyl sulfoxide (15 mL), KI (0.13 g, 0.784 mmol), NaCN (0.769 g, 15.686 mmol) were added and the reaction was subjected to heating at 140° C. for 5 h. The reaction mixture was quenched with ice cold water (50 mL) and extracted with ethyl acetate (2×70 mL). The combined extracts were washed with brine, dried and concentrated. The resulting crude product was purified by normal silica gel (100-200 mesh) column chromatography using 15% ethyl acetate in hexane as eluent to get (1-pyridin-2-yl-cyclopentyl)-acetonitrile (434) (1.2 g, 82%) as a colorless liquid.

Workup

  1. customThe reaction mixture was quenched with ice cold water (50 mL)
  2. extractionextracted with ethyl acetate (2×70 mL)
  3. washThe combined extracts were washed with brine
  4. customdried
  5. concentrationconcentrated
  6. customThe resulting crude product was purified by normal silica gel (100-200 mesh) column chromatography

Sources & evidence

ORD record
ord-11e8526af7434962991d2fd8ed533215
Source dataset
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09045486B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes