Acetic Acid → HCID 12506855, compound

HRID 2101567Notes

Reaction equation

HRID 2101567 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]([CH3:20])=[C:9]([C:12](=[O:19])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[C:10]=1[CH3:11])=[O:5])[CH3:2].C(O)(=[O:23])C.O>O1CCCC1>[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]([CH:20]=[O:23])=[C:9]([C:12](=[O:19])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[C:10]=1[CH3:11])=[O:5])[CH3:2]

Participants

5

Reactant 3

HCID 176Acetic AcidHCID 962WaterHCID 683447HCID 683447, compound

Product 1

HCID 12506855HCID 12506855, compoundYield 75%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

A mixture of 4-benzoyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid ethyl ester (4.13 g, 15.2 mmol) and ceric ammonium nitrate (33 g, 4 equiv.) in 50 mL of tetrahydrofuran (THF):acetic acid (HOAc):H2O 1:1:1 was refluxed overnight. The reaction mixture was then cooled, extracted with EtOAc and then basified to pH 9 with sodium carbonate. The organic layer was then washed with brine, dried (MgSO4) and concentrated followed by column chromatography to give 3.25 g (75%) of 4-benzoyl-5-formyl-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester as a yellow solid.

Workup

  1. temperatureThe reaction mixture was then cooled
  2. extractionextracted with EtOAc
  3. washThe organic layer was then washed with brine
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-c7df5a59ef1146d4bae3c9f9a7596a02
Source dataset
uspto-grants-2009_08
Patent number
US07572924B2

Reaction notes

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