Acetone → o-Anisalacetone

HRID 567131Notes

Reaction equation

HRID 567131 reaction equation
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH:5]=O.[OH-].[Na+].O.C(OCC)(=O)C.[CH3:20][C:21]([CH3:23])=[O:22]>>[CH3:1][O:2][C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH:5]=[CH:20][C:21](=[O:22])[CH3:23]

Participants

6

Reactant 5

HCID 180AcetoneHCID 962WaterHCID 86582-MethoxybenzaldehydeHCID 8857Ethyl AcetateHCID 14798Sodium Hydroxide

Product 1

HCID 139181o-AnisalacetoneYield 82.3%

Procedure

In a 250 ml single neck flask was charged 13.6 g (100 mmoles,1.0 eq) of o-methoxybenzaldehyde dissolved in 30 ml of acetone. To this was added 5 g of 10% aqueous sodium hydroxide solution (12.5 mmoles, 0.125 eq), dropwise and during the course of addition, temperature was kept no higher than 25° C., while the mixture was agitated continuously for 30 minutes. To the mixture was added 50 ml of water, followed by 100 ml of ethyl acetate, the phases were separated and the organic phase was washed with water three times and then dried, and concentrated to obtain 14.5 g of 4-(2-methoxyphenyl)-3-buten-2-one as a faintly yellow oil in 82.3% yield.

Workup

  1. additiondropwise and during the course of addition, temperature
  2. customwas kept no higher than 25° C., while the mixture
  3. customthe phases were separated
  4. washthe organic phase was washed with water three times
  5. customdried
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-621265a941cc4a0f82c157dd4ce3f47b
Source dataset
uspto-grants-2001_01
Patent number
US06177462B1

Reaction notes

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