HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-2-(methylthio)pyridine → 5-Bromo-2-methanesulfonylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-2-(methylthio)pyridine | HCID 11424251 | — |
| Reactant | Magnesium 2-(dioxidan-2-ide-1-carbonyl)benzoate--water (1/1/6) | HCID 21894687 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-2-methanesulfonylpyridine | HCID 13433424 | 92% |
Reaction Steps
5-bromo-2-methylsulfanyl pyridine (3.47 g) was dissolved in a mixed solvent of dichloromethane and methanol with the ratio of 5:1 (v/v) and magnesium monoperoxyphthalate hexahydrate was slowly added dropwise. After completing the reaction for 3 hours at room temperature, magnesium monoperoxyphthalate hexahydrate was filtered out, sodium bicarbonate and salt water was added to dilute, and extracted with dichloromethane to separate an organic layer. The separated organic layer was dried with anhydrous magnesium sulfate and distilled under reduced pressure. As a result, 5-bromo-2-methylsulfonyl pyridine (3.7 g, yield: 92%) was obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06946558B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-df17a300a0d6499e9f3c2d8eac9914c3 |
| Source note | uspto-grants-2005_09 |