Dimethylformamide → HCID 13861691, compound

HRID 1066629Notes

Reaction equation

HRID 1066629 reaction equation
C([Si](C)(C)[O:6][C:7]1[C:8]([F:23])=[C:9]([CH:12]=[C:13](O[Si](C(C)(C)C)(C)C)[CH:14]=1)[CH:10]=[O:11])(C)(C)C.[F-].[K+].[CH3:28]I.CN([CH:33]=[O:34])C>O>[F:23][C:8]1[C:7]([O:6][CH3:28])=[CH:14][C:13]([O:34][CH3:33])=[CH:12][C:9]=1[CH:10]=[O:11]

Participants

6

Reactant 4

HCID 6228DimethylformamideHCID 6328Methyl iodideHCID 522689Potassium FluorideHCID 138616903,5-Bis{[tert-butyl(dimethyl)silyl]oxy}-2-fluorobenzaldehyde

Product 1

HCID 13861691HCID 13861691, compoundYield 60%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A mixture of the 3,5-bis-(tert-butyl-dimethyl-silanyloxy)-2-fluoro-benzaldehyde (3.0 g, 7.8 mmol) obtained in Example 251.1, potassium fluoride (1.81 g, 31.2 mmol), methyl iodide (1.17 ml, 18.7 mmol) and DMF (25 ml) was stirred for 2 h. at room temperature. Water (25 ml) was added and the mixture was extracted with diethyl ether. The organic phase was washed with water, dried, filtered and concentrated. The residue was purified by chromato-graphy (SiO2, cyclohexane/EtOAc 18:1=>1:1). There was obtained 0.87 g (60%) of 2-fluoro-3,5-dimethoxy-benzaldehyde as a colorless solid.

Workup

  1. extractionthe mixture was extracted with diethyl ether
  2. washThe organic phase was washed with water
  3. customdried
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe residue was purified by chromato-graphy (SiO2, cyclohexane/EtOAc 18:1=>1:1)

Sources & evidence

ORD record
ord-5f623bc892e447cd8aaa52b49a14453c
Source dataset
uspto-grants-2001_06
Patent number
US06242644B1

Reaction notes

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