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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3-hydroxybenzoate | HCID 24522 | — |
| Reactant | 1,3-Dioxolane, 2-(bromomethyl)- | HCID 78068 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-((1,3-dioxolan-2-yl)methoxy)benzoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09127314B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-3a9addc8dfb94a4c8338750b1fb79caf |
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| Source note | uspto-grants-2015_09 |
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