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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210901Generated: October 30, 2026

Chloromethyl ethyl ether → 1-Ethoxymethyl-5-ethyluracil

https://huagongshe.com/reaction/2210901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl ethyl etherHCID 18523—
Reactant5-Ethyl-2,4(1H,3H)-pyrimidinedioneHCID 73267—
ReactantSodium BicarbonateHCID 516892—
CatalystTetrabutylammonium IodideHCID 67553—
CatalystBistrimethylsilylacetamidHCID 11708267—
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 (0.88 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 carefully into 50 ml of saturated aqueous solution of sodium hydrogencarbonate 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 numberUS05461060
Source datasetuspto-grants-1995_10
ORD IDord-101120b90e514f79ad12fb9b5de3cf08
Source noteuspto-grants-1995_10