Sodium Sulfate → (5-methyl-1-pyridin-2-yl-1H-pyrazol-4-yl)-methanol
Reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].C([O:9][C:10]([C:12]1[CH:13]=[N:14][N:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][N:19]=2)[C:16]=1[CH3:17])=O)C.S([O-])([O-])(=O)=O.[Na+].[Na+]>O1CCCC1>[CH3:17][C:16]1[N:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][N:19]=2)[N:14]=[CH:13][C:12]=1[CH2:10][OH:9]Participants
5
Procedure
Add lithium aluminum hydride (0.225 g, 5.92 mmol) to tetrahydrofuran (15 mL) at 0° C. then slowly add 5-methyl-1-pyridin-2-yl-1H-pyrazole-4-carboxylic acid ethyl ester (0.685 g, 2.96 mmol) in tetrahydrofuran (5 mL) dropwise. Warm the mixture to room temperature and stir for two hr. then cool the solution to 0° C. Add saturated aqueous sodium sulfate (0.5 mL), warm to room temperature then stir for 2 hr. Filter off the solid materials then dry the solution (sodium sulfate), filter and concentrate to give (5-methyl-1-pyridin-2-yl-1H-pyrazol-4-yl)-methanol as a white solid (0.501 g, 89%).
Workup
- temperaturethen cool the solution to 0° C
- stirringthen stir for 2 hr
- filtrationFilter off the solid materials
- dry with materialthen dry the solution (sodium sulfate)
- filtrationfilter
- concentrationconcentrate
Sources & evidence
- ORD record
- ord-c2c43f674bbd4e9d89b43b5a09e20bcd
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07910588B2
Reaction notes
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