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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387839Generated: October 30, 2026

Potassium Iodide → Ethyl 3-oxo-2-(4-((tetrahydro-2H-pyran-2-yloxy)methyl)benzyl)butanoate

https://huagongshe.com/reaction/2387839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantEthyl AcetoacetateHCID 8868—
ReactantSodium hydrideHCID 24758—
Reactant2-(4-(chloromethyl)benzyloxy)tetrahydro-2H-pyranHCID 10490262—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-oxo-2-(4-((tetrahydro-2H-pyran-2-yloxy)methyl)benzyl)butanoateHCID 68414491—

Reaction Steps

Ethyl acetoacetate (11.7 ml) was added to a stirred suspension of sodium hydride (60% disp. in oil, 3.8 g) in THF (200 ml) at 0° C. under nitrogen. After 1 h, a solution of 2-(4-(chloromethyl)benzyloxy)tetrahydro-2H-pyran (22.2 g) in THF (50 ml) was added, the mixture warmed to rt, then potassium iodide (16 g) added and heated under reflux for 48 h. The mixture was partitioned between water and ether, the organics separated, washed with water, dried and evaporated under reduced pressure. The residue was purified by column chromatography eluting with 20% EtOAc in isohexane to afford the subtitle compound, 15.66 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268990B2
Source datasetuspto-grants-2012_09
ORD IDord-56ba53265f7e4da887688d41a174072e
Source noteuspto-grants-2012_09