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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627781Generated: October 25, 2026

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

https://huagongshe.com/reaction/1627781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethylphosphoramideHCID 12679—
Reactant1-IodopropaneHCID 33643—
ReactantEthyl 2-methyl-1,3-dioxolane-2-propionateHCID 70332—
ReactantLithium diisopropylamineHCID 45051747—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-((2-methyl-1,3-dioxolan-2-yl)methyl)pentanoateHCID 5872530985.1%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785638B2
Source datasetuspto-grants-2014_07
ORD IDord-09a1289354ea4c0c82459690074912f1
Source noteuspto-grants-2014_07