HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (2-Bromo-3-pyridyl)methyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (2-Bromopyridin-3-yl)methanol | HCID 14761460 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2-Bromo-3-pyridyl)methyl methanesulfonate | HCID 58268552 | — |
Reaction Steps
Triethylamine (8.90 mL) is added to a round bottom flask containing a solution of (2-bromopyridin-3-yl)methanol (8 g, 42.55 mmol) in dichloromethane (212 mL) at 0° C., then methanesulfonyl chloride (3.95 mL) is added and the mixture is stirred at that temperature for 1.5 h. After that time the mixture is washed with water and organic layer is decanted, dried over magnesium sulfate and solvent evaporated under reduced pressure to yield 10.4 g of the title compound used without further purification. MS (m/z): 266, 268 (M+1; M+3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08232289B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-593bcd02dce941f9b453c909b64faf74 |
| Source note | uspto-grants-2012_07 |