Sodium Chloride → 5-Methoxy-3-pyridinecarboxaldehyde
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
Reactant 4
Product 1
Reagents, catalysts & solvents 1
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
- temperature5.85 mL, 14.6 mmol) dropwise whilst maintaining an internal temperature <−94° C
- additionThe solution was then poured into sat'd
- extractionand extracted with diethyl ether (3×100 mL)
- dry with materialthe ethereal phase dried (K2CO3)
- filtrationfiltered
- customevaporated in vacuo
- 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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