Potassium Iodide → HCID 23113981, compound

HRID 1787138Notes

Reaction equation

HRID 1787138 reaction equation
[CH:1]([C:4]1[CH:19]=[CH:18][C:7]([CH2:8][C:9]2[C:14]([CH3:15])=[CH:13][C:12]([CH3:16])=[CH:11][C:10]=2[OH:17])=[CH:6][CH:5]=1)([CH3:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+].Cl[CH2:27][C:28](=[O:30])[CH3:29].[I-].[K+]>CC(C)=O.O>[CH:1]([C:4]1[CH:19]=[CH:18][C:7]([CH2:8][C:9]2[C:14]([CH3:15])=[CH:13][C:12]([CH3:16])=[CH:11][C:10]=2[O:17][CH2:27][C:28]([CH3:29])=[O:30])=[CH:6][CH:5]=1)([CH3:3])[CH3:2]

Participants

7

Procedure

A mixed solution of 2-(4-isopropylbenzyl)-3,5-dimethylphenol obtained in Reference Example 148 (1.0 g, 3.93 mmol), potassium carbonate (1.30 g, 9.44 mmol), chloroacetone (436 mg, 4.72 mmol) and potassium iodide (100 mg) in acetone (15 mL) was heated under reflux for 16 hours. Water was added to the reaction solution, which was extracted with ethyl acetate. The combined organic layer was washed with a saturated brine, dried over anhydrous sodium sulfate, filtered, and then concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:4) to obtain 888 mg (yield 73%) of the title compound. Oily matter.

Workup

  1. temperaturewas heated
  2. temperatureunder reflux for 16 hours
  3. extractionwas extracted with ethyl acetate
  4. washThe combined organic layer was washed with a saturated brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customthe obtained residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:4)

Sources & evidence

ORD record
ord-841553179ead41ae92fb9726a38fef87
Source dataset
uspto-grants-2009_03
Patent number
US07507841B2

Reaction notes

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