Reaktion #5343

ord-a7cf8eaa48de44358d5af939538ff052

Reaktionsgleichung

O=C1COC(=O)C1
tetronic acid
CCN(CC)CC
triethylamine
CCN=C=NCCCN(C)C.Cl
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
CCCCCC/C=C\CCCCCCCC(=O)O
palmitoleic acid
Cl
HCl
CCCCCC/C=C\CCCCCCCC(=O)C1=C(O)COC1=O
4-hydroxy-3-((Z)-1-oxo-9-hexadecenyl)-2(5H)-furanone
Ausbeute 36.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with four 100 mL portions of ethyl acetate
  2. 2
    TrocknenThe combined organic layers are dried over MgSO4
  3. 3
    Einengenconcentrated in vacuo
  4. 4
    Sonstigeaffording crude compound

Vorschrift

To a stirring solution of 1.07 g (10.72 mmol) of tetronic acid in 30 mL of dimethylformamide is added 1.64 mL (11.97 mmol) of triethylamine and 428 mg of 4-dimethylaminopyridine at 0° C. Next, 2.44 g (12.77 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 3.0 g (11.79 mmol) of palmitoleic acid are added and the reaction is stirred for 3 days at room temperature. The reaction is acidified with 1.0N HCl and extracted with four 100 mL portions of ethyl acetate. The combined organic layers are dried over MgSO4 and concentrated in vacuo affording crude compound. Pure material was obtained by flash chromatography with 10% methanol/ethyl acetate as eluant affording 1.3 g (36%) of 4-hydroxy-3-((Z)-1-oxo-9-hexadecenyl)-2(5H)-furanone.

Quelle

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