Reaction #1121738

ord-f09c0bd07120450aa5703d5a695dd117

Reaction equation

O=C1CCC(=O)O1
Succinic anhydride
CCCCC/C=C\C/C=C\CCCCCCCCOCCC(O)CN(C)C
1-(dimethylamino)-4-((9Z,12Z)-octadeca-9,12-dienyloxy)butan-2-ol
CCCCC/C=C\C/C=C\CCCCCCCCOCCC(CN(C)C)OC(=O)CCC(=O)O
4-(1-(dimethylamino)-4-((9Z,12Z)-octadeca-9,12-dienyloxy)butan-2-yloxy)-4-oxobutanoic acid

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperaturethe resultant was refluxed for 18 hours under argon
  2. 2
    ConcentrationThe mixture was concentrated
  3. 3
    Otherthe residue was partitioned between EtOAc (10 mL) and deionized water (20 mL)
  4. 4
    OtherThe layers were separated
  5. 5
    Extractionthe aqueous layer was extracted with two additional portions of EtOAc (25 mL)
  6. 6
    DryingThe combined organic extracts were dried (MgSO4)
  7. 7
    Filtrationfiltered
  8. 8
    Concentrationconcentrated

Procedure

Succinic anhydride (0.60 g, 5.99 mmol, 1.1 equiv) was added in one portion to a dry THF (11 mL) solution of 1-(dimethylamino)-4-((9Z,12Z)-octadeca-9,12-dienyloxy)butan-2-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 the residue was partitioned between EtOAc (10 mL) and 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-(1-(dimethylamino)-4-((9Z,12Z)-octadeca-9,12-dienyloxy)butan-2-yloxy)-4-oxobutanoic acid, a thick, yellow oil, which was used without further purification.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08545876B1uspto-grants-2013_10