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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276336Generated: October 26, 2026

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

https://huagongshe.com/reaction/2276336

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 tetrahydrofurane (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 sulfate, 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. ESI/APCI(+): 231 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09132129B2
Source datasetuspto-grants-2015_09
ORD IDord-fd8c823b307d4e839e5045cae5217768
Source noteuspto-grants-2015_09