Water → 4-[2-(3-bromophenyl)-2-oxo-acetyl]-1H-pyrrole-2-carbonitrile

HRID 646263Notes

Reaction equation

HRID 646263 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([C:8]#[C:9][C:10]2[CH:11]=[C:12]([C:15]#[N:16])[NH:13][CH:14]=2)[CH:5]=[CH:6][CH:7]=1.S([O-])([O-])(=O)=[O:18].[Mg+2].C(=O)(O)[O-].[Na+].[O-][Mn](=O)(=O)=O.[K+].[OH2:34]>CC(C)=O.CCOC(C)=O.C(OCC)(=O)C.CCCCCC>[Br:1][C:2]1[CH:3]=[C:4]([C:8](=[O:18])[C:9]([C:10]2[CH:11]=[C:12]([C:15]#[N:16])[NH:13][CH:14]=2)=[O:34])[CH:5]=[CH:6][CH:7]=1

Participants

9

Procedure

A solution of 4-(3-bromo-phenylethynyl)-1H-pyrrole-2-carbonitrile (2.85 g, 10.52 mmol) in acetone was treated with a 45° C. solution of magnesium sulfate (1.90 g, 15.78 mmol) and sodium bicarbonate (0.53 g, 6.31 mmol) in water, immediately treated with KMnO4 (3.74 g, 23.67 mmol), stirred for 15 minutes (TLC (silica gel, 25% ethyl acetate/hexane) indicated complete clean conversion), diluted with EtOAc and washed with water until the washings were colorless. The organic phase was dried (MgSO4), filtered and evaporated. The resultant residue was crystallized to purity from warm ethyl acetate/hexane to afford 4-[2-(3-bromophenyl)-2-oxo-acetyl]-1H-pyrrole-2-carbonitrile as a yellow crystalline solid, 2.68 g, 84% yield.

Workup

  1. washwashed with water until the washings
  2. dry with materialThe organic phase was dried (MgSO4)
  3. filtrationfiltered
  4. customevaporated
  5. customThe resultant residue was crystallized to purity
  6. temperaturefrom warm ethyl acetate/hexane

Sources & evidence

ORD record
ord-e55ded96fe654b1892f5d05c1823adfc
Source dataset
uspto-grants-2010_04
Patent number
US07705030B2

Reaction notes

Loading…