Acetic Acid → Methyl 2-{(benzofuran-5-yl)methylene}-3-oxobutyrate

HRID 1066964Notes

Reaction equation

HRID 1066964 reaction equation
[CH:1]([C:3]1[CH:4]=[CH:5][C:6]2[C:7]([CH:11]=1)=NON=2)=O.[C:12]([O:18][CH3:19])(=[O:17])[CH2:13][C:14]([CH3:16])=[O:15].N1CCCCC1.[C:26]([OH:29])(=O)[CH3:27]>C1C=CC=CC=1>[O:29]1[C:26]2[CH:27]=[CH:1][C:3]([CH:11]=[C:13]([C:14](=[O:15])[CH3:16])[C:12]([O:18][CH3:19])=[O:17])=[CH:4][C:5]=2[CH:6]=[CH:7]1

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 7757Methyl acetoacetateHCID 8082PiperidineHCID 2776296Benzo(c)(1,2,5)oxadiazole-5-carbaldehyde

Product 1

HCID 54375059Methyl 2-{(benzofuran-5-yl)methylene}-3-oxobutyrate

Reagents, catalysts & solvents 1

HCID 241BenzeneSolvent

Procedure

A mixture of 5-Formylbenzofurazan (0.6 g, 4.1 mmol), methyl acetoacetate (0.52 g, 4.5 mmol), piperidine (0.019 g, 0.225 mmol), and acetic acid (0.014 g, 0.225 mmol) in benzene (30 mL) was stirred and refluxed with a Dean-Stark trap for 8 h. Benzene was evaporated, the residue was dissolved in ethyl acetate (80 mL) and washed with brine (50 mL), saturated potassium bisulfate solution (50 mL), and saturated sodium bicarbonate solution in sequence. The ethyl acetate solution was dried (magnesium sulfate), solvent removed under reduced pressure and the residue was purified by column chromatography (SiO2, EtOAc/hexane, 10%-15%). The product, methyl 2-{(benzofuran-5-yl)methylene}-3-oxobutyrate, was obtained as an oil (0.98 g, 98.3%) and was used in the next step without any further characterization.

Workup

  1. temperaturerefluxed with a Dean-Stark trap for 8 h
  2. customBenzene was evaporated
  3. dissolutionthe residue was dissolved in ethyl acetate (80 mL)
  4. washwashed with brine (50 mL), saturated potassium bisulfate solution (50 mL), and saturated sodium bicarbonate solution in sequence
  5. dry with materialThe ethyl acetate solution was dried (magnesium sulfate), solvent
  6. customremoved under reduced pressure
  7. customthe residue was purified by column chromatography (SiO2, EtOAc/hexane, 10%-15%)

Sources & evidence

ORD record
ord-4119453516d0493384c98ee6e4b75079
Source dataset
uspto-grants-2001_06
Patent number
US06245773B1

Reaction notes

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