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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867574Generated: October 30, 2026

3,4-dihydro-2H-pyran → 1-(2-Tetrahydropyranyl)-4-[2-(2-tetrahydropyranyl)oxyethyl]-2-azetidinone

https://huagongshe.com/reaction/867574

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantEthyl AcetateHCID 8857—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 12769226HCID 12769226—
Solvent1,4-DioxaneHCID 31275—
Product1-(2-Tetrahydropyranyl)-4-[2-(2-tetrahydropyranyl)oxyethyl]-2-azetidinoneHCID 14328984—

Reaction Steps

Under nitrogen and at 25° C., a solution of 4-(2-hydroxyethyl)-2-azetidinone (62 mg, 0.539 mmole) in 0.5 ml of anhydrous p-dioxane is treated with 2,3-dihydropyran (0.98 ml, 1.08 mmoles) and p-toluenesulfonic acid monohydrate (19 mg, 0.10 mmole). The resulting solution is stirred for a period of 60 minutes and then partitioned between 10 ml of 0.5M pH7 phosphate buffer and 10 ml of ethyl acetate. The aqueous phase is extracted a second time with ethyl acetate. The combined ethyl acetate solutions are washed with brine, dried over magnesium sulfate and filtered. The filtrate is evaporated unnder reduced pressure to give 216 mg of crude product. Purification by preparation thick-layer chromtography developing with ethyl acetate gives 80 mg of 1-(2-tetrahydropyranyl)-4-[2-(2-tetrahydropyranyl)oxyethyl]-2-azetidinone as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775669
Source datasetuspto-grants-1988_10
ORD IDord-3987929bf8284584bb3498924706805a
Source noteuspto-grants-1988_10