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Water → 5-Methoxy-3-methyl-1-benzofuran-2-carbaldehyde

HRID 2091010
Notes
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Reaction equation

HRID 2091010 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[O:10][C:9]([C:11](OC)=[O:12])=[C:8]([CH3:15])[C:7]=2[CH:16]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O>O1CCCC1.[O-2].[O-2].[Mn+4]>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[O:10][C:9]([CH:11]=[O:12])=[C:8]([CH3:15])[C:7]=2[CH:16]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 962WaterHCID 13157010Methyl 5-methoxy-3-methyl-1-benzofuran-2-carboxylateHCID 21226445Aluminium lithium hydride

Product 1

HCID 230522235-Methoxy-3-methyl-1-benzofuran-2-carbaldehydeYield 79%

Reagents, catalysts & solvents 2

HCID 178418406HCID 178418406, compoundCatalyst
HCID 8028
Tetrahydrofuran
Solvent
2×

Procedure

To a solution (100 mL) of methyl 5-methoxy-3-methyl-1-benzofuran-2-carboxylate (5.00 g) in tetrahydrofuran was added lithium aluminum hydride (862 mg) at 0° C., and the mixture was stirred for 1.5 hr. Water (860 μL) was added to quench the reaction, 1N aqueous sodium hydroxide solution (860 μL) was added, and the mixture was stirred at room temperature for 1 hr. The resulting insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give a pale-yellow solid. To a solution of the obtained solid in tetrahydrofuran (80 mL) was added active manganese dioxide (21.2 g), and the mixture was stirred at 50° C. overnight. Manganese dioxide was filtered off, and the filtrate was concentrated under reduced pressure to give the title object compound (3.41 g, 79%) as a brown solid.

Workup

  1. customto quench
  2. customthe reaction, 1N aqueous sodium hydroxide solution (860 μL)
  3. additionwas added
  4. stirringthe mixture was stirred at room temperature for 1 hr
  5. filtrationThe resulting insoluble material was filtered off
  6. concentrationthe filtrate was concentrated under reduced pressure
  7. customto give a pale-yellow solid
  8. stirringthe mixture was stirred at 50° C. overnight
  9. filtrationManganese dioxide was filtered off
  10. concentrationthe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-373e48e3eac844048cf3f8866d6fd109
Source dataset
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08436043B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes