HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl butyrate → 5-Ethyl-2-thiouracil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl butyrate | HCID 7762 | — |
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Ethyl-2-thiouracil | HCID 3002042 | 82% |
Reaction Steps
To a suspension of potassium tert-butoxide (12.08 g, 108 mmol) in THF (40 mL) was added a solution of ethyl butyrate (5.69 mL, 43.0 mmol) and ethyl formate (6.93 mL, 86 mmol) in diethyl ether (40.0 mL) dropwise under nitrogen. The mixture was stirred at room temperature for 3 h. After removing the solvent, the residue oil was dissloved in isopropanol (350 mL), and thiourea (6.55 g, 86 mmol) was added. The mixture was stirred at reflux overnight, and then concentrated in vacuo to get a solid. The solid was dissolved in water, adjusted pH to 4 with AcOH, and extracted by DCM. The organic layer was dried over Na2SO4, filtered and concentrated to afford the title compound (5.5 g, 82% yield) as a pink solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637536B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-9ede782568ba4fff862f24bcc82dab25 |
| Source note | uspto-grants-2014_01 |