Methyl formate → 3,5-Difluoropyridine-4-carbaldehyde

HRID 1844181Notes

Reaction equation

HRID 1844181 reaction equation
C([Li])CCC.CCCCCC.C(NC(C)C)(C)C.[F:19][C:20]1[CH:21]=[N:22][CH:23]=[C:24]([F:26])[CH:25]=1.[CH:27](OC)=[O:28].C(=O)(O)[O-].[Na+]>C1COCC1>[F:26][C:24]1[CH:23]=[N:22][CH:21]=[C:20]([F:19])[C:25]=1[CH:27]=[O:28]

Participants

8

Conditions

Temperature
0 °C

Procedure

Under argon and at −70° C., 44 ml of 2.5 M n-butyllithium solution in n-hexane (110 mmol, 1.1 equivalent) were slowly added dropwise to 15.4 ml of diisopropylamine (110 mmol, 1.1 equivalent) in 23 ml of THF. The solution formed was warmed to 0° C. and stirred at this temperature for 30 min. The reaction mixture was then brought to −70° C. and diluted with 23 ml of THF, and 11.5 g of 3,5-difluoropyridine (100 mmol, 1 equivalent) dissolved in 72 ml of THF, were added dropwise. The mixture was stirred at −70° C. for 30 min. 12.4 ml of methyl formate (200 mmol, 2 equivalent), dissolved in 23 ml of THF, were then slowly added dropwise. After 1.5 h at −70° C., the reaction solution was quickly poured into 230 ml of saturated aqueous sodium bicarbonate solution and extracted with a total of 460 ml of ethyl acetate. The combined organic phases were washed twice with in each case 115 ml of saturated aqueous sodium bicarbonate solution and twice with saturated aqueous sodium chloride solution, dried over sodium sulphate and concentrated using a rotary evaporator. This gave 11.6 g (81% of theory) of the title compound which were directly reacted further.

Workup

  1. customThe solution formed
  2. customwas then brought to −70° C.
  3. additionwere added dropwise
  4. stirringThe mixture was stirred at −70° C. for 30 min
  5. additionwere then slowly added dropwise
  6. waitAfter 1.5 h at −70° C.
  7. extractionextracted with a total of 460 ml of ethyl acetate
  8. washThe combined organic phases were washed twice with in each case 115 ml of saturated aqueous sodium bicarbonate solution and twice with saturated aqueous sodium chloride solution
  9. dry with materialdried over sodium sulphate
  10. concentrationconcentrated
  11. customa rotary evaporator
  12. customThis gave 11.6 g (81% of theory) of the title compound which were directly reacted further

Sources & evidence

ORD record
ord-99aaa4ec8ad946759e6508f564f09474
Source dataset
uspto-grants-2015_02
Patent number
US08946215B2

Reaction notes

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