Sodium Chloride → 5-Methoxy-3-pyridinecarboxaldehyde

HRID 751432Notes

Reaction equation

HRID 751432 reaction equation
Br[C:2]1[CH:3]=[N:4][CH:5]=[C:6]([O:8][CH3:9])[CH:7]=1.C([Li])CCC.CN([CH:18]=[O:19])C.[Na+].[Cl-]>C(OCC)C>[CH:18]([C:2]1[CH:3]=[N:4][CH:5]=[C:6]([O:8][CH3:9])[CH:7]=1)=[O:19]

Participants

6

Conditions

Temperature
-60 °C

Procedure

To a solution of 3-Bromo-5-methoxypyridine (2.5 g, 13.3 mmol) in anhydrous diethyl ether cooled to −100° C. was added n-butyllithium (2.5M soln in hexanes: 5.85 mL, 14.6 mmol) dropwise whilst maintaining an internal temperature <−94° C. After subsequent stirring for 30 minutes, anhydrous DMF (1.34 mL, 17.3 mmol) was added and the reaction mixture allowed to warm to −60° C.. The solution was then poured into sat'd. aq. NaCl soln. and extracted with diethyl ether (3×100 mL), the ethereal phase dried (K2CO3), filtered and evaporated in vacuo. The residue was purified on silica gel eluting with a gradient of 0 to 30% EtOAc in hexanes to afford the title material as an oil.

Workup

  1. temperature5.85 mL, 14.6 mmol) dropwise whilst maintaining an internal temperature <−94° C
  2. additionThe solution was then poured into sat'd
  3. extractionand extracted with diethyl ether (3×100 mL)
  4. dry with materialthe ethereal phase dried (K2CO3)
  5. filtrationfiltered
  6. customevaporated in vacuo
  7. customThe residue was purified on silica gel eluting with a gradient of 0 to 30% EtOAc in hexanes

Sources & evidence

ORD record
ord-3cf95453dab6431dba644fcd21ce2bba
Source dataset
uspto-grants-2008_07
Patent number
US07405302B2

Reaction notes

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