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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057252Generated: October 26, 2026

Chloromethyl ethyl ether → 1-Ethoxymethyl-5-ethyluracil

https://huagongshe.com/reaction/1057252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl ethyl etherHCID 18523—
Reactant5-Ethyl-2,4(1H,3H)-pyrimidinedioneHCID 73267—
ReactantSodium BicarbonateHCID 516892—
ReactantBistrimethylsilylacetamidHCID 11708267—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDichloromethaneHCID 6344—
Product1-Ethoxymethyl-5-ethyluracilHCID 1026231781%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037979E1
Source datasetuspto-grants-2003_02
ORD IDord-8cc9ce0ee045418088ce1a2501c1672c
Source noteuspto-grants-2003_02