Reaktion #1577180

ord-df2bc10022bb487ea666d50d500e10ac

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted three times with ether
  2. 2
    TrocknenThe combined organic layers are dried over MgSO4
  3. 3
    Einengenconcentrated in vacuo
  4. 4
    Sonstigegiving a yellow solid
  5. 5
    Filtrationfiltering

Vorschrift

To a stirring solution of 554 mg (5.54 mmol) of tetronic acid in 20 mL of dimethylformamide is added 850 μL (6.09 mmol) of triethylamine and 220 mg (1.765 mmol) of 4-dimethylaminopyridine at 0° C. Next, 1.26 g (6.63 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 1.475 g (6.63 mmol) of 6-[4-(hexyloxy)phenoxy]hexanoic acid are added and the reaction mixture is stirred 2 days at room temperature. The reaction is acidified with 1.0N HCI and extracted three times with ether. The combined organic layers are dried over MgSO4 and concentrated in vacuo giving a yellow solid. Pure material is obtained by trituration in ether, filtering to give 774 mg (43%) of 4-hydroxy-3-[6-(4-chlorophenoxy)-1-oxohexyl]-2(5H)-furanone.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05679801uspto-grants-1997_10