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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | Ethyl 2-methyl-1,3-dioxolane-2-propionate | HCID 70332 | — |
| Reactant | Lithium diisopropylamine | HCID 45051747 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-((2-methyl-1,3-dioxolan-2-yl)methyl)pentanoate | HCID 58725309 | 85.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785638B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-09a1289354ea4c0c82459690074912f1 |
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| Source note | uspto-grants-2014_07 |
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