Reaction #5358

ord-07070efa6bb7493ba824bd6a67d62928

Reaction equation

Cl
HCl
O=C1CSC(=O)C1
thiotetronic acid
CCN=C=NCCCN(C)C.Cl
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
CCCCC/C=C\C/C=C\CCCCCCCC(=O)O
linoleic acid
CCCCC/C=C\C/C=C\CCCCCCCC(=O)C1=C(O)CSC1=O
4-hydroxy-3-[(Z,Z)-1-oxo-9,12-octadecadienyl]-2(5H)-thiophenone
Yield 30.0%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Extractionextracted three times with diethyl ether
  2. 2
    WashThe combined organic layers are washed with brine
  3. 3
    Dryingdried over Na2SO4
  4. 4
    Filtrationfiltered
  5. 5
    Concentrationconcentrated in vacuo
  6. 6
    OtherThe residue is recrystallized from pentane at -78° C.
  7. 7
    Otherto give a solid which
  8. 8
    Temperatureupon warming to room temperature

Procedure

To a stirring solution of 1.71 g (14.75 mmol) of thiotetronic acid in 10 mL of dimethylformamide is added 2.22 ML (17.2 mmol) of triethylamine and 592 mg (4.85 mmol) of 4-dimethylaminopyridine at 0° C. Next, 3.38 g (17.6 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 4.96 g (17.7 mmol) of linoleic acid are added and the reaction mixture is stirred overnight at room temperature. The reaction is acidified with 1.0N HCl and extracted three times with diethyl ether. The combined organic layers are washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue is recrystallized from pentane at -78° C. to give a solid which melts upon warming to room temperature giving 1.67 g (30%) of 4-hydroxy-3-[(Z,Z)-1-oxo-9,12-octadecadienyl]-2(5H)-thiophenone as an oil.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05242945uspto-grants-1993_09