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Hydrogen Peroxide → 3-Isopropyl-4-methoxyphenol

HRID 352540
Notes
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Reaction equation

HRID 352540 reaction equation
[CH:1]([C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])C=O)([CH3:3])[CH3:2].S(=O)(=O)(O)[OH:15].OO>CO>[CH:1]([C:4]1[CH:5]=[C:6]([OH:15])[CH:9]=[CH:10][C:11]=1[O:12][CH3:13])([CH3:3])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 784Hydrogen PeroxideHCID 1118Sulfuric AcidHCID 98989903-Isopropyl-4-methoxybenzaldehyde

Product 1

HCID 113326753-Isopropyl-4-methoxyphenol

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a solution of 3-isopropyl-4-methoxybenzaldehyde (12.5 g, 70 mmol) in MeOH(140 mL) was added concentrated sulfuric acid (1.2 mL) followed by dropwise addition of 30% by wt aqueous hydrogen peroxide(6 g, 20 mL, 176 mmol). The mixture was left to stir at ambient room temperature. After 3 hours, the mixture was concentrated in vacuo to about ⅓ of the reaction volume. The concentrate was partitioned between EtOAc (100 mL) and brine (50 mL). The EtOAc extract was washed with brine (50 mL), dried (Na2SO4), filtered and concentrated in vacuo to give 13.5 g of dark oil as crude product. The crude product was purified by chromatography (250 g silica gel, 10% EtOAc in hexane) to afford 10.1 g (86%) of compound 1c as a thick oil that eventually solidified.

Workup

  1. waitThe mixture was left
  2. concentrationthe mixture was concentrated in vacuo to about ⅓ of the reaction volume
  3. customThe concentrate was partitioned between EtOAc (100 mL) and brine (50 mL)
  4. extractionThe EtOAc extract
  5. washwas washed with brine (50 mL)
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-27f9263d92614b00bf75248c61ec0cfe
Source dataset
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06747048B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes