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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617185Generated: November 2, 2026

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

https://huagongshe.com/reaction/1617185

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 numberUS08765939B2
Source datasetuspto-grants-2014_07
ORD IDord-ff79f9e2d9954695a848b3af94dfc6e0
Source noteuspto-grants-2014_07