Dimethyl Sulfoxide → 3-(4-Methoxyphenyl)propanal

HRID 1257767Notes

Reaction equation

HRID 1257767 reaction equation
CS(C)=O.C(Cl)(=O)C(Cl)=O.[CH3:11][O:12][C:13]1[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][CH2:21][OH:22])=[CH:15][CH:14]=1.C(N(CC)CC)C>ClCCl>[CH3:11][O:12][C:13]1[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][CH:21]=[O:22])=[CH:15][CH:14]=1

Participants

6

Conditions

Temperature
-78 °C

Procedure

A solution of dimethyl sulfoxide (5.1 mL) in dichloromethane (10 ml) was added to a stirred solution of oxalyl chloride (3.0 mL, 36 mmol) in dichloromethane (40 ml) at −78° C. over 30 min. Upon completion of the addition, the mixture was stirred at −78° C. for 5 min, followed by addition of a solution of 4-methoxybenzenepropanol (3.0 g, 18 mmol) in dichloromethane (20 ml) at −78° C. over 30 min. The resulting mixture was stirred at −78° C. for 40 min. Next, triethylamine (15 mL, 110 mmol) was added dropwise over 10 min. The resulting mixture was allowed to warm to 0° C. and stirred at this temperature for 1 hour. It was diluted with dichloromethane (30 mL) and quenched with water (15 mL). The organic extracts were separated, washed with water and brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography eluting with ethyl acetate in hexanes (gradient: 3 min: 0/100 to 23 min: 20/80) to afford the desired product (1.50 g, 51%).

Workup

  1. additionUpon completion of the addition
  2. stirringThe resulting mixture was stirred at −78° C. for 40 min
  3. temperatureto warm to 0° C.
  4. stirringstirred at this temperature for 1 hour
  5. customquenched with water (15 mL)
  6. customThe organic extracts were separated
  7. washwashed with water and brine
  8. dry with materialdried over magnesium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure
  11. customThe residue was purified by flash chromatography
  12. washeluting with ethyl acetate in hexanes (gradient: 3 min: 0/100 to 23 min: 20/80)

Sources & evidence

ORD record
ord-c76f52c7a20b4b9d9be124c56f3cf171
Source dataset
uspto-grants-2013_06
Patent number
US08461330B2

Reaction notes

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