HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloromethyl ethyl ether → 1-Ethoxymethyl-5-ethyluracil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloromethyl ethyl ether | HCID 18523 | — |
| Reactant | 5-Ethyl-2,4(1H,3H)-pyrimidinedione | HCID 73267 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Bistrimethylsilylacetamid | HCID 11708267 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Ethoxymethyl-5-ethyluracil | HCID 10262317 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE037979E1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-8cc9ce0ee045418088ce1a2501c1672c |
| Source note | uspto-grants-2003_02 |