HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → [5-(3-[1,3]Dioxan-2-yl-phenylsulfanyl)-4-fluoro-2-nitro-phenyl]-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | (4,5-Difluoro-2-nitrophenyl)methanol | HCID 57475722 | — |
| Reactant | 3-[1,3]Dioxan-2-yl-benzenethiol | HCID 57864083 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [5-(3-[1,3]Dioxan-2-yl-phenylsulfanyl)-4-fluoro-2-nitro-phenyl]-methanol | HCID 86634266 | — |
Reaction Steps
3-[1,3]Dioxan-2-yl-benzenethiol (2.57 g, 14.02 mmol), prepared as described in Example 1, Step C, (4,5-difluoro-2-nitro-phenyl)-methanol (2.65 g, 14.02 mmol), and cesium carbonate (9.1 g, 28 mmol) were combined in DMF (100 mL). The resulting mixture was stirred overnight at room temperature. Water was added, and the resulting mixture was then extracted with ethyl acetate. The organic layer was dried with Na2SO4 and filtered, and the solvent was removed to yield an oil, which was purified via silica column chromatography (50% EtOAc/heptane) to yield a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076358B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-60138009a16e4b00b2599e700f5a3aee |
| Source note | uspto-grants-2011_12 |