Water → 4'-Formyl-[1,1'-biphenyl]-2-carbonitrile

HRID 277475Notes

Reaction equation

HRID 277475 reaction equation
Br[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:16]=[CH:15][CH:14]=[CH:13][C:10]=2[C:11]#[N:12])=[CH:5][CH:4]=1.C(=O)(O)[O-:18].[Na+].O>CS(C)=O>[CH:2]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:16]=[CH:15][CH:14]=[CH:13][C:10]=2[C:11]#[N:12])=[CH:5][CH:4]=1)=[O:18]

Participants

5

Reactant 3

HCID 962WaterHCID 516892Sodium BicarbonateHCID 15019124'-(Bromomethyl)-2-cyanobiphenyl

Product 1

HCID 13940624'-Formyl-[1,1'-biphenyl]-2-carbonitrileYield 63.1%

Reagents, catalysts & solvents 1

HCID 679Dimethyl SulfoxideSolvent

Conditions

Temperature
120 °C

Procedure

A mixture of 2-(4-bromomethylphenyl)benzonitrile (12 g) and sodium bicarbonate (26 g) in dimethyl sulfoxide (150 ml) was heated at 120° C. for 5 hours with stirring. After addition of water, the mixture was extracted with ethyl acetate. The extract was washed with water, dried and concentrated to dryness. The residue was purified by column chromatography on silica gel to give crystals. Recrystallization from chloroform-isopropyl ether gave colorless needles (5.77 g, 63%).

Workup

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe extract was washed with water
  3. customdried
  4. concentrationconcentrated to dryness
  5. customThe residue was purified by column chromatography on silica gel
  6. customto give crystals
  7. customRecrystallization from chloroform-isopropyl ether

Sources & evidence

ORD record
ord-47848f8028fc4cfea598248963ace00d
Source dataset
uspto-grants-2002_03
Patent number
US06355808B2

Reaction notes

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