Réaction #1121730
ord-a6108a594ce945dab537ccccccce5210
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1Températurethe resultant was refluxed for 18 hours under argon
- 2ConcentrationThe mixture was concentrated
- 3Autrethe residue was partitioned between EtOAc (10 mL) and deionized water (20 mL)
- 4AutreThe layers were separated
- 5Extractionthe aqueous layer was extracted with two additional portions of EtOAc (25 mL)
- 6SéchageThe combined organic extracts were dried (MgSO4)
- 7Filtrationfiltered
- 8Concentrationconcentrated
Mode opératoire
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-oxobutanoicacid, a thick, yellow oil, which was used without further purification.