Sodium borohydride → HCID 86649115, compound

HRID 2364862Notes

Reaction equation

HRID 2364862 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:22])[CH2:9][CH2:10][C:11]([C:13]2[CH:18]=[CH:17][C:16]([N+:19]([O-:21])=[O:20])=[CH:15][CH:14]=2)=[O:12])=[CH:4][C:3]=1[N+:23]([O-:25])=[O:24].[BH4-].[Na+]>CCO>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([OH:22])[CH2:9][CH2:10][CH:11]([C:13]2[CH:14]=[CH:15][C:16]([N+:19]([O-:21])=[O:20])=[CH:17][CH:18]=2)[OH:12])=[CH:4][C:3]=1[N+:23]([O-:25])=[O:24]

Participants

4

Reactant 2

HCID 4311764Sodium borohydrideHCID 86649114HCID 86649114, compound

Product 1

HCID 86649115HCID 86649115, compoundYield 92%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

To a solution of the product from Example 179A (10.0 g, 27.6 mmol) in EtOH (220 mL) was added sodium borohydride (2.190 g, 57.9 mmol) in several portions over 1 h. The resulting mixture was stirred at rt for 1 h, filtered through celite, and concentrated in vacuo. The residue was dissolved in EtOAc and washed by 1N aq. HCl. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo to give the title compound (9.29 g, 92%)

Workup

  1. filtrationfiltered through celite
  2. concentrationconcentrated in vacuo
  3. dissolutionThe residue was dissolved in EtOAc
  4. washwashed by 1N aq. HCl
  5. dry with materialThe organic layer was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-f5bf6f4dcc23431da5c3826b7a597797
Source dataset
uspto-grants-2014_04
Patent number
US08691938B2

Reaction notes

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