HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoromethyluracil → 5-trifluoromethyl-2,4-bis(trimethylsilyloxy)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoromethyluracil | HCID 5899 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Solvent | Hexamethyldisilazane | HCID 13838 | — |
| Product | 5-trifluoromethyl-2,4-bis(trimethylsilyloxy)pyrimidine | HCID 10990962 | — |
Reaction Steps
In 50 ml of hexamethyldisilazane, 6.16 g of 5-trifluoromethyluracil was suspended and then 0.22 ml of trimethylchlorosilane was added to the suspension, followed by heating the resulting mixture to reflux for 5 hours. After the reaction, the excess hexamethyldisilazane was removed by evaporation and the resultant was distilled in vacuum. All of the fractions of distillate obtained at about 60° C. under 1 mmHg were collected. Yield: 10.3 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05532349 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-584c1ea662e0478e8b7213f4c54bf5ae |
| Source note | uspto-grants-1996_07 |