Ammonium formate → HCID 59786574, compound
Reaction equation
C([O-])=O.[NH4+].[CH3:5][O:6][C:7]1[CH:12]=[C:11]([CH:13]([OH:19])[CH:14]([N+:16]([O-])=O)[CH3:15])[CH:10]=[CH:9][N:8]=1>[Pd].C1COCC1.CO>[NH2:16][CH:14]([CH3:15])[CH:13]([C:11]1[CH:10]=[CH:9][N:8]=[C:7]([O:6][CH3:5])[CH:12]=1)[OH:19]Participants
6
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Procedure
Ammonium formate (1.13 g, 18 mmol) and palladium on charcoal (10%, 175 mg) is added to a solution of 1-(2-methoxypyridin-4-yl)-2-nitro-propan-1-ol (760 mg, 3.6 mmol) in 17.5 ml THF and 17.5 ml methanol. The reaction mixture is stirred overnight at room temperature, filtered through a path of cellites and concentrated. Yield 620 mg of a racemic mixture of two diastereomers, 95%.
Workup
- filtrationfiltered through a path of cellites
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-0bcc57bac2684be0a386d93ae9b3b200
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08030340B2
Reaction notes
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