Aluminium lithium hydride → HCID 67126802, compound
Reaction equation
[F:1][C:2]1([C:12](OCC)=[O:13])[CH2:7][CH2:6][N:5]([CH:8]2[CH2:11][O:10][CH2:9]2)[CH2:4][CH2:3]1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[F:1][C:2]1([CH2:12][OH:13])[CH2:3][CH2:4][N:5]([CH:8]2[CH2:9][O:10][CH2:11]2)[CH2:6][CH2:7]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of EXAMPLE 357A (0.59 g) in tetrahydrofuran (5 mL) was added lithium aluminum hydride (1.80 mL) at 0° C. The reaction was removed from the ice bath and allowed to warm to room temperature. The reaction was quenched by the dropwise addition of 0.6 ml of water followed by 0.2 ml of 2N aqueous NaOH. The reaction was filtered through celite and rinsed with ethyl acetate (50 mL). The mixture and the residue was loaded onto silica gel (Reveleris 40 g) and eluted using a gradient of 0.75% to 7.5% methanol/dichloromethane over 30 minutes (flow=40 mL/minutes) to provide the title compound.
Workup
- customThe reaction was removed from the ice bath
- customThe reaction was quenched by the dropwise addition of 0.6 ml of water
- filtrationThe reaction was filtered through celite
- washrinsed with ethyl acetate (50 mL)
- washeluted
- customover 30 minutes
Sources & evidence
- ORD record
- ord-7a8ea1c83e8046ffaf24e38aefc9c2a4
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09034875B2
Reaction notes
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