HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 5-Iodo-6-(trifluoromethyl)pyrimidin-4(3H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 4-Hydroxy-6-(trifluoromethyl)pyrimidine | HCID 135458620 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Iodo-6-(trifluoromethyl)pyrimidin-4(3H)-one | HCID 136066338 | 8.5% |
Reaction Steps
N-Iodosuccinimide (2.75 g) was added to a stirred suspension of 4-trifluoromethylpyrimidin-6-one (1 g) in dry acetonitril (13 ml). The reaction mixture was stirred at the ambient temperature for 2 hours, and then heated under reflux for 10 hours. After cooling, removal of the solvent under reduced pressure gave a brown solid which was recrystallised from water to give 5-iodo-4-trifluoromethylpyrimidin-6-one as a pale orange solid (150 mg);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05149810 |
| Source dataset | uspto-grants-1992_09 |
| ORD ID | ord-8dabd6c5e4a8483d9ec805f25bc45a6e |
| Source note | uspto-grants-1992_09 |