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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275697Generated: October 29, 2026

Sodium Iodide → Ethyl 3-((1,3-dioxolan-2-yl)methoxy)benzoate

https://huagongshe.com/reaction/2275697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-hydroxybenzoateHCID 24522—
Reactant1,3-Dioxolane, 2-(bromomethyl)-HCID 78068—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-((1,3-dioxolan-2-yl)methoxy)benzoateHCID 17999177—

Reaction Steps

2-Bromomethyl-1,3-dioxolane (8.3 ml, 80 mmol), ethyl-3-hydroxy-benzoate (3.32 g, 20 mmol), potassium carbonate (5.53 g, 40 mmol) and sodium iodide (1.2 g, 8 mmol) were heated at 120° C. in DMF (8 ml) for 17 hrs. The reaction was cooled to room temperature and all the solvents were evaporated under reduced pressure. The residues were partitioned between DCM (250 ml) and water (250 ml). The DCM layer was separated and the aqueous layer was back-extracted with DCM (2×100 ml). All the DCM extracts were combined, dried over MgSO4 and evaporated under reduced pressure. The residue was purified by column chromatography (4×25 cm). The product was eluted with 20% petroleum ether (60-80° C.) in DCM and the title compound was obtained as a slightly brown oil (4.63 g, 91.8%). APCI-MS, m/z 252.95 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09127314B2
Source datasetuspto-grants-2015_09
ORD IDord-3a9addc8dfb94a4c8338750b1fb79caf
Source noteuspto-grants-2015_09