Ethanol → 3-Bromo-5-ethoxypyridine
Reaction equation
Br[C:2]1[CH:3]=[N:4][CH:5]=[C:6]([Br:8])[CH:7]=1.[CH2:9]([OH:11])[CH3:10]>>[Br:8][C:6]1[CH:5]=[N:4][CH:3]=[C:2]([O:11][CH2:9][CH3:10])[CH:7]=1Participants
3
Procedure
Ethanol and 3,5-dibromopyridine were processed as described in Example 7A to provide the title compound (69% yield). MS (DCI/NH3) m/z 202/204 (M+H)+.
Sources & evidence
- ORD record
- ord-03854ec3411848e09220b9c71b80218f
- Source dataset
- uspto-grants-2004_10
- Patent number
- US06809105B2
Reaction notes
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