HCID 19385657, compound → HCID 19385618, compound

HRID 2255602Notes

Reaction equation

HRID 2255602 reaction equation
[Si:1]([O:8][C:9]1[C:18]([Cl:19])=[CH:17][C:12]([C:13](OC)=[O:14])=[CH:11][C:10]=1[Cl:20])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[Si:1]([O:8][C:9]1[C:10]([Cl:20])=[CH:11][C:12]([CH2:13][OH:14])=[CH:17][C:18]=1[Cl:19])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]

Participants

4

Procedure

To a stirred and cooled (0° C.) solution of 7.70 g (23.0 mmol) of the product of Step A dissolved in 50 mL of anhydrous THF was added 23.0 mL (23.0 mmol) of a 1M solution of lithium aluminum hydride in THF. After the addition was complete the reaction mixture was allowed to warm to room temperature and stirred 3.5 hours. The stirred reaction was then quenched by dropwise addition of 0.88 mL water, then 0.88 mL of 15% NaOH, and finally 2.62 mL water. The reaction mixture was then filtered and concentrated in vacuo. The residue was dissolved in ethyl acetate, washed with 1N HC1, saturated NaHCO3, dried (MgSO4), and evaporated in vacuo to afford 1.83 g (26%) of the title compound.

Workup

  1. additionAfter the addition
  2. stirringstirred 3.5 hours
  3. customThe stirred reaction
  4. customwas then quenched by dropwise addition of 0.88 mL water
  5. filtrationThe reaction mixture was then filtered
  6. concentrationconcentrated in vacuo
  7. dissolutionThe residue was dissolved in ethyl acetate
  8. washwashed with 1N HC1, saturated NaHCO3
  9. dry with materialdried (MgSO4)
  10. customevaporated in vacuo

Sources & evidence

ORD record
ord-bb8a27b6237042c8b439488a2a513a64
Source dataset
uspto-grants-1993_08
Patent number
US05240938

Reaction notes

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