Reacción #1121728
ord-f80910c7050e4fdaab66ea7a7b4c51fd
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturathe resultant was refluxed for 18 hours under argon
- 2ConcentraciónThe mixture was concentrated
- 3workup.DISSOLUTIONdissolved in EtOAc (10 mL)
- 4workup.ADDITIONpoured into deionized water (20 mL)
- 5OtroThe layers were separated
- 6Extracciónthe aqueous layer was extracted with two additional portions of EtOAc (25 mL)
- 7SecadoThe combined organic extracts were dried (MgSO4)
- 8Filtraciónfiltered
- 9Concentraciónconcentrated
Procedimiento
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.