Water → 2-(4-Bromo-2-fluorophenyl)acetonitrile

HRID 2387056Notes

Reaction equation

HRID 2387056 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8]Br)=[C:4]([F:10])[CH:3]=1.[C-:11]#[N:12].[Na+].O.C([O-])(O)=O.[Na+]>CN(C=O)C.CCOC(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:11]#[N:12])=[C:4]([F:10])[CH:3]=1

Participants

7

Conditions

Temperature
70 °C

Procedure

To a solution of 4-bromo-1-bromomethyl-2-fluoro-benzene (8.15 g, 30.4 mmol) dissolved in DMF (16 mL) were added sodium cyanide (2.24 g, 45.6 mmol) and water (2 mL). The reaction was stirred for one hour at 70° C. To the reaction was added 130 mL water; 120 mL saturated NaHCO3, and 100 mL EtOAc. The layers were separated, and the aqueous layer was extracted with 3×100 mL EtOAc. The combined organics were washed with 100 mL water, and then dried over Na2SO4. After filtering off the solids, the mother liquor was concentrated to the desired product by rotary evaporation (6.5 g, 99% yield). MS (APCI): 240 (M+H), 242 (M+2+H).

Workup

  1. customThe layers were separated
  2. extractionthe aqueous layer was extracted with 3×100 mL EtOAc
  3. washThe combined organics were washed with 100 mL water
  4. dry with materialdried over Na2SO4
  5. filtrationAfter filtering off the solids
  6. concentrationthe mother liquor was concentrated to the desired product by rotary evaporation (6.5 g, 99% yield)

Sources & evidence

ORD record
ord-54b1df58a40d480d8aaf727139c0d573
Source dataset
uspto-grants-2012_09
Patent number
US08268835B2

Reaction notes

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