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Ozone → Methyl benzofuran-7-carboxylate

HRID 342084
Notes
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Reaction equation

HRID 342084 reaction equation
O=[O+][O-].[CH2:4]([C:7]1[CH:16]=[CH:15][CH:14]=[C:9]([C:10]([O:12][CH3:13])=[O:11])[C:8]=1[OH:17])[CH:5]=C>>[O:17]1[C:8]2[C:9]([C:10]([O:12][CH3:13])=[O:11])=[CH:14][CH:15]=[CH:16][C:7]=2[CH:4]=[CH:5]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24823OzoneHCID 208027Methyl 2-hydroxy-3-(2-propen-1-yl)benzoate

Product 1

HCID 14229730Methyl benzofuran-7-carboxylateYield 44%

Procedure

Ozone was bubbled through a solution of methyl 3-allyl-salicylate (30 g, 156 mmol) at -78° C. for 2 hr until no starting material was present on TLC. The reaction was quenched with dimethyl sulfide and stirred at room temperature for 18 hr. The mixture was concentrated in vacuo, and the residue was dissolved in ether. The ether solution was washed with brine three times, and then concentrated in vacuo to a green oil. This oil was dissolved in toluene and heated to reflux with sulfuric acid (0.5 ml) for 4 hr. Sodium carbonate (5 g) was added, and the mixture was cooled and then filtered. The filtrated was concentrated in vacuo to a dark oil that was purified by chromatography on silica gel using methylene chloride as the eluent to give the product as a green oil (12 g, 44%).

Workup

  • customThe reaction was quenched with dimethyl sulfide
  • concentrationThe mixture was concentrated in vacuo
  • dissolutionthe residue was dissolved in ether
  • washThe ether solution was washed with brine three times
  • concentrationconcentrated in vacuo to a green oil
  • dissolutionThis oil was dissolved in toluene
  • temperatureheated
  • temperatureto reflux with sulfuric acid (0.5 ml) for 4 hr
  • additionSodium carbonate (5 g) was added
  • temperaturethe mixture was cooled
  • filtrationfiltered
  • concentrationThe filtrated was concentrated in vacuo to a dark oil that
  • customwas purified by chromatography on silica gel
  • Sources & evidence

    ORD record
    ord-c5cda2b7265140feb2b705b8073fc877
    Source dataset
    uspto-grants-1999_01
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05856529

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes