Sodium Cyanide → m-Chlorophenylacetonitrile

HRID 254809

Reaction equation

HRID 254809 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5]Br.[C-:10]#[N:11].[Na+]>C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]([CH2:5][C:10]#[N:11])[CH:7]=[CH:8][CH:9]=1

Participants

4

Procedure

The experimental procedure was followed by the method of Bruno P. Imbimbo et al [J. Med. Chem. 2005, 48, 5707-7520]. A solution of 3-chlorobenzylbromide (5 g, 24.3 mmol) and sodium cyanide (1.3 g, 26.8 mmol) in ethanol (50 ml) was heated to 80° C. for 2 hours. After resulting solution was cooled to room temperature and concentrated under reduced pressure. The residue was suspended in water and organic layer was extracted with ethyl acetate. The solution was evaporated and crude compound was purified by silica gel column chromatography (hexane/ethyl acetate=5/1) to yield 2-(3-chlorophenyl)acetonitrile (3.2 g, 87% yield) as colorless oil.

Workup

  1. customAfter resulting solution
  2. concentrationconcentrated under reduced pressure
  3. extractionorganic layer was extracted with ethyl acetate
  4. customThe solution was evaporated
  5. customcrude compound was purified by silica gel column chromatography (hexane/ethyl acetate=5/1)

Sources & evidence

ORD record
ord-8947ee673ebb41428f9ec878f3d5b2cd
Source dataset
uspto-grants-2011_01
Patent number
US07875647B2

Linked notes

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