3-Furanol, tetrahydro- → 5-Bromo-4-methyl-2-(oxolan-3-yloxy)pyridine
Reaction equation
[Br:1][C:2]1[C:3]([CH3:9])=[CH:4][C:5]([OH:8])=[N:6][CH:7]=1.O[CH:11]1[CH2:15][CH2:14][O:13][CH2:12]1>>[Br:1][C:2]1[C:3]([CH3:9])=[CH:4][C:5]([O:8][CH:11]2[CH2:15][CH2:14][O:13][CH2:12]2)=[N:6][CH:7]=1Participants
3
Procedure
The title compound was prepared from 5-bromo-2-hydroxy-4-methylpyridine and rac-3-hydroxy-tetrahydrofuran in analogy to Example 9c): colorless liquid.
Sources & evidence
- ORD record
- ord-4e03017035f54862b15fe2e4f5e1896d
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367838B2
Reaction notes
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