HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (2-Fluoropyridin-3-yl)methyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Fluoro-3-(hydroxymethyl)pyridine | HCID 14761461 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2-Fluoropyridin-3-yl)methyl methanesulfonate | HCID 86634652 | — |
Reaction Steps
A solution of (2-fluoropyridin-3-yl)methanol (400 mg, 3.1 mmol), methanesulfonyl chloride (0.37 mL, 4.7 mmol) and triethylamine (0.88 mL, 6.30 mmol) in dichloromethane (10 mL) was stirred at rt for 16 h. The mixture was then diluted with dichloromethane and washed with H2O, then brine. The organic phase was collected, dried (MgSO4) and concentrated in vacuo to give (2-fluoropyridin-3-yl)methyl methanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242987B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-5fb0a970e0324ed3a251cb256e4adeca |
| Source note | uspto-grants-2016_01 |