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

HRID 235165Notes

Reaction equation

HRID 235165 reaction equation
C(Cl)(=O)C(Cl)=O.CS(C)=O.[CH2:11]([C:23]1[CH:27]=[C:26]([CH2:28][OH:29])[O:25][N:24]=1)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22]>ClCCl>[CH2:11]([C:23]1[CH:27]=[C:26]([CH:28]=[O:29])[O:25][N:24]=1)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22]

Participants

5

Conditions

Temperature
-60 °C

Procedure

A solution of oxalyl chloride (28.8 ml) in dry dichloromethane (100 ml) was cooled to -60° C. and a solution of dimethylsulfoxide (8.9 ml) in dichloromethane (30 ml) was added, followed by a slurry of 3-(1-dodecyl)-5-isoxazolemethanol (14.0 g) in dry dichloromethane (200 ml). The mixture was stirred at -60° C. for 1 hr, quenched with triethylamine (87 ml) and allowed to warm to room temperature. The solution was poured into water (300 ml) and extracted with dichloromethane. The organic phases were washed with dilute citric acid solution, dried, filtered, and the filtrate was evaporated. The residue was passed through a short pad of silica gel using dichloromethane as the eluent. The solution was evaporated and the residue was recrystallized from ether-hexane to give 11.5 g (78%) of product, mp 53°-54° C.

Workup

  1. customquenched with triethylamine (87 ml)
  2. temperatureto warm to room temperature
  3. additionThe solution was poured into water (300 ml)
  4. extractionextracted with dichloromethane
  5. washThe organic phases were washed with dilute citric acid solution
  6. customdried
  7. filtrationfiltered
  8. customthe filtrate was evaporated
  9. customThe solution was evaporated
  10. customthe residue was recrystallized from ether-hexane

Sources & evidence

ORD record
ord-ec2471d80a1346bab41a18af61adf093
Source dataset
uspto-grants-1997_01
Patent number
US05597838

Reaction notes

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