Sodium Iodide → 2'-Fluoro-2-(1-hydroxy-2,2-dimethyl-but-3-enyl)-5'-methoxy-biphenyl-4-carboxylic acid methyl ester

HRID 1662422Notes

Reaction equation

HRID 1662422 reaction equation
[I-].[Na+].[In].Br[CH2:5][CH:6]=[C:7]([CH3:9])[CH3:8].[CH3:10][O:11][C:12]([C:14]1[CH:19]=[CH:18][C:17]([C:20]2[CH:25]=[C:24]([O:26][CH3:27])[CH:23]=[CH:22][C:21]=2[F:28])=[C:16]([CH:29]=[O:30])[CH:15]=1)=[O:13]>CN(C=O)C.CCOC(C)=O.O>[CH3:10][O:11][C:12]([C:14]1[CH:19]=[CH:18][C:17]([C:20]2[CH:25]=[C:24]([O:26][CH3:27])[CH:23]=[CH:22][C:21]=2[F:28])=[C:16]([CH:29]([OH:30])[C:7]([CH3:9])([CH3:8])[CH:6]=[CH2:5])[CH:15]=1)=[O:13]

Participants

8

Procedure

To a mixed solution of sodium iodide (2080 mg, 13876 μmol), indium (2000 mg, 6938 μmol) and 1-bromo-3-methylbut-2-ene (1616 μL, 13876 μmol) in DMF (30 mL), was added 66.41C (1593 mg, 13876 μmol). The mixture was stirred at room temperature for 1 hour, and then was diluted with EtOAc and water. The organic phase was washed with water and brine and then dried over anhydrous sodium sulfate. After filtration, the organic solvent was removed in vacuo to give a residue which was purified by chromatography to give the product as an oil (2.30 g, 92%). MS ESI m/e: 376.1 (M+18)+.

Workup

  1. washThe organic phase was washed with water and brine
  2. dry with materialdried over anhydrous sodium sulfate
  3. filtrationAfter filtration
  4. customthe organic solvent was removed in vacuo
  5. customto give a residue which
  6. customwas purified by chromatography

Sources & evidence

ORD record
ord-2cd620b0601b4550abe6c5c7d1f5956e
Source dataset
uspto-grants-2011_10
Patent number
US08030354B2

Reaction notes

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