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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 725219Erstellt: 25. Oktober 2026

3,4-dihydro-2H-pyran → 2-Propanone, 1,3-bis[(tetrahydro-2H-pyran-2-yl)oxy]-

https://huagongshe.com/reaction/725219

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4-dihydro-2H-pyranHCID 8080—
Edukt1,4-DioxaneHCID 31275—
EduktSodium BicarbonateHCID 516892—
EduktDihydroxyacetone dimerHCID 4180364—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
Produkt2-Propanone, 1,3-bis[(tetrahydro-2H-pyran-2-yl)oxy]-HCID 11010660—

Reaktionsschritte

9 g of 2,5-dihydroxy-1,4-dioxane-2,5-dimethanol were introduced into 60 ml of dioxane and the suspension was taken to about 70° C. for 15 minutes, then taken to ambient temperature. Then, 20 ml of 3,4-dihydro-2H-pyran and 300 mg of monohydrated p-toluene sulfonic acid were added. The temperature was held at about 40° C. and then the reaction medium stood overnight at ambient temperature. It was then poured into a mixture of 300 ml of a saturated solution of sodium bicarbonate+10 ml of triethylamine and extraction was carried out 4 times with methylene chloride. The organic phase was washed with salt water and dried. After purification by passing through silica with ethyl cycloacetate/triethylamine: 8/2 as eluant, 17 g of the expected product (pale yellow syrup) were obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05705654
Quelldatensatzuspto-grants-1998_01
ORD IDord-4db769bb2ed64288a6bcedb8e40fba6f
Quellennotizuspto-grants-1998_01