Dimethyl Sulfoxide → 3-(1-Decyl)-5-isoxazolecarboxaldehyde

HRID 1734801Notes

Reaction equation

HRID 1734801 reaction equation
C(Cl)(=O)C(Cl)=O.CS(C)=O.[CH2:11]([C:21]1[CH:25]=[C:24]([CH2:26][OH:27])[O:23][N:22]=1)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]>ClCCl>[CH2:11]([C:21]1[CH:25]=[C:24]([CH:26]=[O:27])[O:23][N:22]=1)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]

Participants

5

Conditions

Temperature
-60 °C

Procedure

To a solution of oxalyl chloride (31.7 ml) in dry dichloromethane (100 ml) cooled to -60° C., was added a solution of dimethylsulfoxide (9.8 ml) in dichloromethane (30 ml) followed by a slurry of 3-(1-decyl)-5-isoxazolemethanol (13.8 g) in dry dichloromethane (100 ml). The reaction mixture was stirred at -60° C. for 0.5 hr, quenched with triethylamine (40 ml), and allowed to warm to ambient temperature. The solution was poured into water (300 ml) and extracted with dichloromethane. The organic phases were washed with dilute citric acid, dried, and evaporated. The residue was flash chromatographed (silica, 50:1-dichloromethane:methanol). The appropriate fraction were collected and evaporated. The residue was recrystallized from ether-hexane to give 11.2 g (82%) of product, mp 46°-48° C.

Workup

  1. customquenched with triethylamine (40 ml)
  2. temperatureto warm to ambient temperature
  3. additionThe solution was poured into water (300 ml)
  4. extractionextracted with dichloromethane
  5. washThe organic phases were washed with dilute citric acid
  6. customdried
  7. customevaporated
  8. customchromatographed (silica, 50:1-dichloromethane:methanol)
  9. customThe appropriate fraction were collected
  10. customevaporated
  11. customThe residue was recrystallized from ether-hexane

Sources & evidence

ORD record
ord-fe217a1eda874c4ba47f2b3621b72836
Source dataset
uspto-grants-1996_07
Patent number
US05534636

Reaction notes

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