Dimethyl Sulfoxide → 7-[4-(4-Methoxyphenyl)thiazol-2-yl]heptanal

HRID 1039150Notes

Reaction equation

HRID 1039150 reaction equation
CS(C)=O.C(Cl)(=O)C(Cl)=O.[CH3:11][O:12][C:13]1[CH:18]=[CH:17][C:16]([C:19]2[N:20]=[C:21]([CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][OH:31])[S:22][CH:23]=2)=[CH:15][CH:14]=1.C(N(CC)CC)C>C(Cl)Cl.C(OCC)(=O)C>[CH3:11][O:12][C:13]1[CH:14]=[CH:15][C:16]([C:19]2[N:20]=[C:21]([CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH:30]=[O:31])[S:22][CH:23]=2)=[CH:17][CH:18]=1

Participants

7

Procedure

Add anhydrous dimethyl sulfoxide (0.25 mL, 3.52 mmol) dropwise over 2 minutes to a solution of oxalyl chloride (393 mg, 3.10 mmol) in methylene chloride (10 mL) at −78° C. under nitrogen and stir the mixture for 20 minutes. Add a solution of 7-[4-(4-methoxyphenyl)thiazol-2-yl]heptan-1-ol (0.609 g, 1.99 mmol) in methylene chloride (10 mL) dropwise in 5 minutes and then stir the mixture for 30 minutes. To this mixture, add triethylamine (1.0 mL, 7.2 mmol), stir and warm the reaction mixture to room temperature for 40 minutes. Dilute the mixture with ethyl acetate (100 mL), wash with brine (3×30 mL), dry over sodium sulfate and remove the solvent under reduced pressure to provide 7-[4-(4-methoxyphenyl)thiazol-2-yl]heptanal (0.6 g, 99%): APCI mass spectrum m/z 304 [C17H21NO2S+H]+.

Workup

  1. stirringstir the mixture for 30 minutes
  2. stirringstir
  3. washwash with brine (3×30 mL)
  4. dry with materialdry over sodium sulfate
  5. customremove the solvent under reduced pressure

Sources & evidence

ORD record
ord-a846079e05814dffaa1138e77518a905
Source dataset
uspto-grants-2013_10
Patent number
US08552039B2

Reaction notes

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