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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1627781Erstellt: 26. Oktober 2026

Hexamethylphosphoramide → Ethyl 2-((2-methyl-1,3-dioxolan-2-yl)methyl)pentanoate

https://huagongshe.com/reaction/1627781

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexamethylphosphoramideHCID 12679—
Edukt1-IodopropaneHCID 33643—
EduktEthyl 2-methyl-1,3-dioxolane-2-propionateHCID 70332—
EduktLithium diisopropylamineHCID 45051747—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 2-((2-methyl-1,3-dioxolan-2-yl)methyl)pentanoateHCID 5872530985,1%

Reaktionsschritte

To a cooled (−78° C.) solution of lithium diisopropylamine (30 mL; 60 mmol; 2N in THF) in THF (8 mL) was added hexamethylphosphoramide (12 mL) and the solution was stirred for 30 min. A solution of ethyl 3-(2-methyl-1,3-dioxolan-2-yl)propanoate (9.4 g; 50 mmol), in THF (9 mL), was added over 30 min and stirring was continued for 1 h. Propyl iodide (6.84 mL; 70 mmol) was slowly added and the solution was allowed to warm to room temperature for 4 h. the reaction was quenched by adding a saturated aqueous solution of ammonium chloride. The two phases were separated and the aqueous layer was extracted with ethyl acetate (50 mL) and the combined organic layers were dried with sodium sulphatesulphate, filtered and concentrated under reduced pressure. The crude residue was purified by flash-chromatography on silica gel using a gradient of ethyl acetate (0-40%) in heptane to furnish 9.8 g (85%) of ethyl 2-((2-methyl-1,3-dioxolan-2-yl)methyl)pentanoate as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08785638B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-09a1289354ea4c0c82459690074912f1
Quellennotizuspto-grants-2014_07