Sodium Iodide → 2-Bromobenzene-1-carbonyl cyanide

HRID 2249047Notes

Reaction equation

HRID 2249047 reaction equation
[I-].[Na+].[Br:3][C:4]1[CH:12]=[CH:11][CH:10]=[CH:9][C:5]=1[C:6](Cl)=[O:7].[C:13](#[N:15])C>>[Br:3][C:4]1[CH:12]=[CH:11][CH:10]=[CH:9][C:5]=1[C:6]([C:13]#[N:15])=[O:7]

Participants

4

Reactant 3

HCID 5238Sodium IodideHCID 6342AcetonitrileHCID 235422-Bromobenzoyl chloride

Product 1

HCID 129692022-Bromobenzene-1-carbonyl cyanide

Procedure

The reaction was carried out under Argon. Cuprous cyanide (6.52q, 72.8 mmol) and anhydrous sodium iodide (20.25g, 135 mmol) were stirred for 2 minutes in anhydrous acetonitrile (100 ml). The resulting solution was mixed with o-bromo benzoyl chloride (15.0q, 68 mmol) whereupon an orange precipitate formed. The mixture was stirred for 30 minutes at room temperature, filtered and concentrated in vacuo. The residue was taken up in dichloromethane and the resulting precipitate was filtered off. Concentration of the filtrate under reduced pressure gave a yellow solid. Recrystallisation from 60°-80° C. b.p.t. petroleum ether afforded o-bromo benzoyl cyanide as yellow crystals (7.14q, 50%), meltinq point 64° C.

Workup

  1. customformed
  2. filtrationfiltered
  3. concentrationconcentrated in vacuo
  4. filtrationthe resulting precipitate was filtered off
  5. customConcentration of the filtrate under reduced pressure gave a yellow solid
  6. customRecrystallisation from 60°-80° C. b.p.t

Sources & evidence

ORD record
ord-5b92836972654527aa4eff5e4079828f
Source dataset
uspto-grants-1991_08
Patent number
US05041681

Reaction notes

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