Aluminium lithium hydride → HCID 178463772, compound
Reaction equation
[CH3:1][CH:2]([CH3:19])[CH:3]([NH:15][C:16](=O)[CH3:17])[C:4]1[NH:5][CH:6]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:8]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[CH2:16]([NH:15][CH:3]([C:4]1[NH:5][CH:6]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:8]=1)[CH:2]([CH3:19])[CH3:1])[CH3:17]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of N-[2-methyl-1-(4-phenyl-1H-imidazol-2-yl)-propyl]-acetamide (0.077 g, 0.30 mmol) in THF (2.0 mL) was added dropwise over 10 min to a refluxing 1.0 M solution of LiAlH4 in THF (3.0 mL). The reaction was maintained at reflux for 11 h, cooled to rt, and quenched by sequential treatment with 0.11 mL of cold water (5° C.), 0.11 mL of 15% NaOH in aqueous solution, and 0.33 mL of cold water (5° C.). The resultant solid was removed by suction filtration and the filtrate (pH 8-9) was extracted three times with EtOAc. The combined organic fractions were dried over MgSO4, filtered, and concentrated to afford 0.069 g of a 5:1 mixture (determined by 1H NMR) of ethyl-[2-methyl-1-(4-phenyl-1H-imidazol-2-yl)-propyl]-amine and recovered
Workup
- temperatureThe reaction was maintained
- temperatureat reflux for 11 h
- customquenched by sequential treatment with 0.11 mL of cold water (5° C.), 0.11 mL of 15% NaOH in aqueous solution, and 0.33 mL of cold water (5° C.)
- customThe resultant solid was removed by suction filtration
- extractionthe filtrate (pH 8-9) was extracted three times with EtOAc
- dry with materialThe combined organic fractions were dried over MgSO4
- filtrationfiltered
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-fdbfe7bc5fe24028b90ce5f6cf63f6e3
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08772325B2
Reaction notes
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