Dimethyl Sulfoxide → HCID 11078038, compound

HRID 234214Notes

Reaction equation

HRID 234214 reaction equation
C(Cl)(=O)C(Cl)=O.CS(C)=O.[C:11]([O:30][CH2:31][CH2:32][CH2:33][CH2:34][OH:35])([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(N(CC)CC)C>ClCCl.O>[C:11]([O:30][CH2:31][CH2:32][CH2:33][CH:34]=[O:35])([C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1)([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

Participants

7

Reactant 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 3717024-trityloxybutan-1-ol

Product 1

HCID 11078038HCID 11078038, compoundYield 79.8%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6344DichloromethaneSolvent3×

Conditions

Temperature
-70 °C

Procedure

To a solution of 43.9 g of oxalyl chloride in 0.52 l of dichloromethane, pre-cooled to -70° C., was added over 35 min a solution of 62.9 g of dimethylsulfoxide in 0.10 l of dichloromethane. The solution was stirred for 10 min at -70° C. Then, a solution of 76.5 g of 4-trityloxy-1-butanol in 0.3 l of dichloromethane was added over 35 min, the temperature being maintained at -65° to -70° C. Stirring was continued for another 20 min, and then, 92.9 g of triethylamine were added over 10 min at -60° to -70° C. The mixture was stirred for 20 min at -70° C., and then allowed to warm to 20° C. over 45 min. After the addition of 0.5 l of water, stirring was continued for 15 min. The layers were separated and the aqueous phase was extracted with 0.6 l of dichloromethane. The organic phase was washed with 0.6 l of water and dried over sodium sulfate, and the solvent was evaporated in vacuo. The residue was crystallized from hexane to yield 60.7 g of 4-trityloxy-butanal as white crystals of m.p. 62°-65° C.

Workup

  1. temperaturethe temperature being maintained at -65° to -70° C
  2. stirringStirring
  3. waitwas continued for another 20 min
  4. stirringThe mixture was stirred for 20 min at -70° C.
  5. temperatureto warm to 20° C. over 45 min
  6. stirringstirring
  7. waitwas continued for 15 min
  8. customThe layers were separated
  9. extractionthe aqueous phase was extracted with 0.6 l of dichloromethane
  10. washThe organic phase was washed with 0.6 l of water
  11. dry with materialdried over sodium sulfate
  12. customthe solvent was evaporated in vacuo
  13. customThe residue was crystallized from hexane

Sources & evidence

ORD record
ord-8e467438feed46be8444891128121676
Source dataset
uspto-grants-1997_01
Patent number
US05594135

Reaction notes

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