Aluminium lithium hydride → HCID 67126802, compound

HRID 1036063Notes

Reaction equation

HRID 1036063 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]1

Participants

4

Reactant 2

HCID 21226445Aluminium lithium hydrideHCID 67126714HCID 67126714, compound

Product 1

HCID 67126802HCID 67126802, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a solution of EXAMPLE 372A (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 diatomaceous earth and rinsed with ethyl acetate (50 mL). The organics were concentrated and loaded onto silica gel (Reveleris 40 g) and eluted using a gradient of 0.75% to 7.5% methanol/dichloromethane over 30 minute (flow=40 mL/minutes) to give the title compound.

Workup

  1. customThe reaction was removed from the ice bath
  2. customThe reaction was quenched by the dropwise addition of 0.6 mL of water
  3. filtrationThe reaction was filtered through diatomaceous earth
  4. washrinsed with ethyl acetate (50 mL)
  5. concentrationThe organics were concentrated and loaded onto silica gel (Reveleris 40 g)
  6. washeluted
  7. customover 30 minute

Sources & evidence

ORD record
ord-0196f396de4e46a196a9a5a88645ed08
Source dataset
uspto-grants-2013_10
Patent number
US08546399B2

Reaction notes

Loading…