Reacción #1121738
ord-f09c0bd07120450aa5703d5a695dd117
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturathe resultant was refluxed for 18 hours under argon
- 2ConcentraciónThe mixture was concentrated
- 3Otrothe residue was partitioned between EtOAc (10 mL) and deionized water (20 mL)
- 4OtroThe layers were separated
- 5Extracciónthe aqueous layer was extracted with two additional portions of EtOAc (25 mL)
- 6SecadoThe combined organic extracts were dried (MgSO4)
- 7Filtraciónfiltered
- 8Concentraciónconcentrated
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 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.