Reaction #5367

ord-b671135f8fab4cebb2baed92c5498047

Reaction equation

O=C1COC(=O)C1
tetronic acid
CCN(CC)CC
triethylamine
CCN=C=NCCCN(C)C.Cl
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
CCCCCCCCCCCCCCCC(=O)O
palmitic acid
Cl
HCl
CCCCCCCCCCCCCCCC(=O)C1=C(O)COC1=O
4-hydroxy-3-[1-oxohexadecyl]-2(5H)-furanone
Yield 91.0%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Extractionextracted three times with ethyl acetate
  2. 2
    WashThe combined organic layers are washed with brine
  3. 3
    Dryingdried over MgSO4
  4. 4
    Concentrationconcentrated in vacuo
  5. 5
    OtherThe residue is recrystallized from pentane

Procedure

To a stirring solution of 650 mg (6.5 mmol) of tetronic acid in 20 mL of dimethylformamide is added 1.0 mL (7.17 mmol) of triethylamine and 230 mg (1.88 mmol) of 4-dimethylaminopyridine at 0° C. Next, 1.50 g (7.81 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 2.0 g (7.81 mmol) of palmitic 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 ethyl acetate. The combined organic layers are washed with brine, dried over MgSO4, and concentrated in vacuo. The residue is recrystallized from pentane to give 2.0 g (91%) of 4-hydroxy-3-[1-oxohexadecyl]-2(5H)-furanone, mp 81°-83° C.

Source

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