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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1057252Erstellt: 27. Oktober 2026

Chloromethyl ethyl ether → 1-Ethoxymethyl-5-ethyluracil

https://huagongshe.com/reaction/1057252

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloromethyl ethyl etherHCID 18523—
Edukt5-Ethyl-2,4(1H,3H)-pyrimidinedioneHCID 73267—
EduktSodium BicarbonateHCID 516892—
EduktBistrimethylsilylacetamidHCID 11708267—
KatalysatorTetrabutylammonium IodideHCID 67553—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-Ethoxymethyl-5-ethyluracilHCID 1026231781%

Reaktionsschritte

To 100 ml of methylene chloride, 5.1 g (40 mmol) of 5-ethyluracil and 22 ml (88 mmol) of bistrimethylsilylacetamide were added under a nitrogen atmosphere and stirred for 40 minutes at room temperature. To this mixture, 4.1 ml (88 mmole) of chloromethyl ethyl ether and 0.15 g (0.4 mmol) of tetrabutylammonium iodide were added and heated under reflux for 15 hours. Then, the reaction mixture was poured into 50 ml of saturated sodium bicarbonate solution carefully and filtered through Celite. The organic layer was washed with water, dried on magnesium sulfate and concentrated under reduced pressure. The residue was crystallized from ethyl acetate to obtain 6.4 g of 1-ethoxymethyl-5-ethyluracil (Yield: 81%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE037979E1
Quelldatensatzuspto-grants-2003_02
ORD IDord-8cc9ce0ee045418088ce1a2501c1672c
Quellennotizuspto-grants-2003_02