Water → HCID 69060363, compound

HRID 2103055Notes

Reaction equation

HRID 2103055 reaction equation
[CH2:1]([C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([CH:9]([CH3:11])[CH3:10])[C:4]=1[OH:12])[CH3:2].[OH2:13]>>[CH2:1]([C:3]1[CH:8]=[C:7]([OH:13])[CH:6]=[C:5]([CH:9]([CH3:11])[CH3:10])[C:4]=1[OH:12])[CH3:2]

Participants

3

Procedure

To a solution of K2S2O8 (8.2 g) in 80 mL of water, was added at once a solution of the above 2-ethyl-6-isopropylphenol (2 g, 12.2 mmol in 25 mL 5% NaOH solution). The mixture was stirred for 3 h and extracted with hexane (3×60 mL). The organic extract was stirred with Na2S2SO4 solution (8.5 g, in 100 mL water) for one hour and the layers were separated. The organic layer was dried over Na2S2O4 and concentrated and dried under high vacuum to give 2-ethyl-6-isopropylbenzene-1,4-diol. To a solution of the crude 2-ethyl-6-isopropylbenzene-1,4-diol in dichloromethane (50 mL) was added acetyl chloride (2.9 g, 36 mmol) and then triethylamine (6 g, 60 mmol) slowly at 0° C. The mixture was stirred at room temperature for 2 h and diluted with hexane/EtOAc (4:1). The mixture was filtered and the filtrate was washed with water (3×80 mL) and dried over Na2SO4 and concentrated. The crude product was purified to afford 2-ethyl-6-isopropyl-1,4-phenylene diacetate as a yellow oil (750 mg).

Workup

  1. extractionextracted with hexane (3×60 mL)
  2. extractionThe organic extract
  3. stirringwas stirred with Na2S2SO4 solution (8.5 g, in 100 mL water) for one hour
  4. customthe layers were separated
  5. dry with materialThe organic layer was dried over Na2S2O4
  6. concentrationconcentrated
  7. customdried under high vacuum

Sources & evidence

ORD record
ord-3b5dbc480d424b3a82cf6c32b321fd57
Source dataset
uspto-grants-2009_08
Patent number
US07576094B2

Reaction notes

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