HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4(1H)-Pyrimidinone, 2-(butylthio)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thiouracil | HCID 1269845 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4(1H)-Pyrimidinone, 2-(butylthio)- | HCID 534218 | — |
Reaction Steps
2-Thioxo-2,3-dihydro-1H-pyrimidin-4-one (12.8 g) was added to a solution of NaOH (8.0 g) in water (70 mL). After complete dissolution of the solids butyl iodide (12.4 mL) was added to the solution and the resulting mixture was stirred at RT overnight. A second aliquot of butyl iodide (1.2 mL) was then added and the reaction mixture was stirred for 24 h. A third aliquot of butyl iodide (1.2 mL) was added and the resulting mixture was stirred for 6 days. Glacial acetic acid (5.5 mL) was added and the reaction mixture was stirred for 30 min, it was then stored at 4° C. overnight. The precipitate formed was collected by filtration and dried under reduced pressure to give 12.3 g of 2-butylsulfanyl-3H-pyrimidin-4-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399462B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-ebb20cb6aad14451816afaa1dea67da8 |
| Source note | uspto-grants-2013_03 |