Reaktion #1121728

ord-f80910c7050e4fdaab66ea7a7b4c51fd

Reaktionsgleichung

O=C1CCC(=O)O1
Succinic anhydride
CCCCC/C=C\C/C=C\CCCCCCCCOC(CO)CN(C)C
3-(dimethylamino)-2-((9Z,12Z)-octadeca-9,12-dienyloxy)propan-1-ol
CCCCC/C=C\C/C=C\CCCCCCCCOC(COC(=O)CCC(=O)O)CN(C)C
4-(3-(dimethylamino)-2-((9Z,12Z)-octadeca-9,12-dienyloxy)propoxy)-4-oxobutanoic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe resultant was refluxed for 18 hours under argon
  2. 2
    EinengenThe mixture was concentrated
  3. 3
    workup.DISSOLUTIONdissolved in EtOAc (10 mL)
  4. 4
    workup.ADDITIONpoured into deionized water (20 mL)
  5. 5
    SonstigeThe layers were separated
  6. 6
    Extraktionthe aqueous layer was extracted with two additional portions of EtOAc (25 mL)
  7. 7
    TrocknenThe combined organic extracts were dried (MgSO4)
  8. 8
    Filtrationfiltered
  9. 9
    Einengenconcentrated

Vorschrift

Succinic anhydride (0.60 g, 5.99 mmol, 1.1 equiv) was added in one portion to a dry THF (11 mL) solution of 3-(dimethylamino)-2-((9Z,12Z)-octadeca-9,12-dienyloxy)propan-1-ol (2.0 g, 5.45 mmol, 1.0 equiv) and the resultant was refluxed for 18 hours under argon. The mixture was concentrated and then dissolved in EtOAc (10 mL) and poured into deionized water (20 mL). The layers were separated and the aqueous layer was extracted with two additional portions of EtOAc (25 mL). The combined organic extracts were dried (MgSO4), filtered and concentrated to provide crude 4-(3-(dimethylamino)-2-((9Z,12Z)-octadeca-9,12-dienyloxy)propoxy)-4-oxobutanoic acid, a thick yellow oil, which was used without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08545877B2uspto-grants-2013_10