HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 50898388, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86667487 | HCID 86667487 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 50898388 | HCID 50898388 | 28% |
Reaction Steps
Compound 3 (41.5 mg, 0.0999 mmol) obtained in Example 3 was dissolved in 1,4-dioxane (3.0 mL), and thionyl chloride (21.9 μL, 0.300 mmol) was added thereto at room temperature, followed by stirring for 1 hour. A saturated aqueous sodium bicarbonate solution was added to the reaction mixture, followed by extraction with ethyl acetate twice. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to yield a residue. The residue was purified by preparative thin layer chromatography to obtain the title compound (11.6 mg, 28%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952003B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-8b424a794fd34442ace64fb08d4d8c3d |
| Source note | uspto-grants-2015_02 |