HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(2,3-Difluorophenyl)-6-(3-chloro-2-propynyloxy)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(2,3-Difluorophenyl)-6-(2-propynyloxy)pyrimidine | HCID 22599853 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Product | 4-(2,3-Difluorophenyl)-6-(3-chloro-2-propynyloxy)pyrimidine | HCID 22599830 | — |
Reaction Steps
In 5 ml of carbon tetrachloride was dissolved 241 mg of 4-(2,3-difluorophenyl)-6-(2-propynyloxy)pyrimidine, to which 136 mg of potassium carbonate and 136 mg of tetra-n-butylammonium chloride were added, followed by stirring at room temperature for 16 hours. The reaction mixture was then poured into water and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated. The resulting residue was subjected to silica gel column chromatography to give 159 mg of 4-(2,3-difluorophenyl)-6-(3-chloro-2-propynyloxy)pyrimidine (the present compound (136)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06838463B2 |
| Source dataset | uspto-grants-2005_01 |
| ORD ID | ord-03aa5239efdd4aa69eb677364a452c45 |
| Source note | uspto-grants-2005_01 |