Dimethyl Sulfoxide → 2-(4-Fluorophenyl)-2-methylpropanal

HRID 1807906Notes

Reaction equation

HRID 1807906 reaction equation
C(Cl)(=O)C(Cl)=O.CS(C)=O.[F:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]([CH3:22])([CH3:21])[CH2:19][OH:20])=[CH:14][CH:13]=1.C(N(CC)CC)C>ClCCl.O>[F:11][C:12]1[CH:13]=[CH:14][C:15]([C:18]([CH3:22])([CH3:21])[CH:19]=[O:20])=[CH:16][CH:17]=1

Participants

7

Conditions

Temperature
-60 °C

Procedure

To a stirred solution of oxalyl chloride (2.81 ml) in dichoromethane (30 ml) at −60° C. was added dropwise a solution of dry dimethyl sulphoxide (4.84 ml) in dichloromethane (20 ml). The mixture was stirred for 15 min at −60° C. and then a solution of 2-(4-fluoro-phenyl)-2-methyl-propan-1-ol (4.59 g; CAS 703-10-6) in dichloromethane (20 ml) was added dropwise. The mixture was stirred at −60° C. for 2 hours and then triethylamine (18.9 ml) was added dropwise. The reaction mixture was allowed to warm to room temperature and diluted with water and with dichloromethane. The phases were separated and the organic phase was washed with water and then dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography (SiO2, heptane/EtOAc gradient) to yield a colourless oil, (3.47 g, 77%).

Workup

  1. stirringThe mixture was stirred at −60° C. for 2 hours
  2. temperatureto warm to room temperature
  3. customThe phases were separated
  4. washthe organic phase was washed with water
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by column chromatography (SiO2, heptane/EtOAc gradient)
  8. customto yield a colourless oil, (3.47 g, 77%)

Sources & evidence

ORD record
ord-fb928b76fc3b413d964918a05317227a
Source dataset
uspto-grants-2013_01
Patent number
US08357712B2

Reaction notes

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