Aluminium lithium hydride → (2S)-2-amino-3-butyl-1-heptanol
Reaction equation
[H-].[H-].[H-].[H-].[Li+].[Al+3].[N:7]([C@@H:10]([CH:26]([CH2:31][CH2:32][CH2:33][CH3:34])[CH2:27][CH2:28][CH2:29][CH3:30])[C:11](N1[C@H](CC2C=CC=CC=2)COC1=O)=[O:12])=[N+]=[N-]>C1COCC1>[NH2:7][C@@H:10]([CH:26]([CH2:31][CH2:32][CH2:33][CH3:34])[CH2:27][CH2:28][CH2:29][CH3:30])[CH2:11][OH:12]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 36 °C
Procedure
To a slurry of LAH (1.219 g, 32.13 mmol) in THF (60 mL) was added (4R)-3-[(2S)-2-azido-3-butylheptanoyl]-4-benzyl-1,3-oxazolidin-2-one (3.6 g, 9.37 mmol) dropwise at 0° C. over 20 min. The reaction was heated to 36° C. for 18 h. The reaction slurry (brown) was cooled to 0° C. and the reaction was quenched with H2O (15 mL) and washed with 1N NaOH (30 mL) and H2O (15 mL). It was let stir for 2 h to obtain an off-white slurry. The slurry was filtered and the mother liquor was further dried over MgSO4, filtered, and concentrated in vacuo to obtain (2S)-2-amino-3-butyl-1-heptanol as a crude yellow oil (1.93 g, 73.75%). Mass Spectrum (+ESI): 188 (M+H)+.
Workup
- temperatureThe reaction slurry (brown) was cooled to 0° C.
- customthe reaction was quenched with H2O (15 mL)
- washwashed with 1N NaOH (30 mL) and H2O (15 mL)
- customto obtain an off-white slurry
- filtrationThe slurry was filtered
- dry with materialthe mother liquor was further dried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-a27a675dbe3f434891158ac9e86d2bbe
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06610734B2
Reaction notes
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