HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → 2-Fluoro-2-methylpropyl trifluoromethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 2-Fluoro-2-methylpropan-1-ol | HCID 11126179 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Fluoro-2-methylpropyl trifluoromethanesulfonate | HCID 12165534 | 85% |
Reaction Steps
Trifluoromethanesulfonic anhydride (12.06 ml, 71.24 mmol), followed by 2,6-lutidine (11.42 ml, 81.42 mmol) were added to a solution of 2-fluoro-2-methylpropan-1-ol (6.25 g, 67.85 mmol) in DCM (146 ml) at −10° C. The reaction was stirred for 1 hr. then washed with 2N HCl (2×100 ml) and saturated NaHCO3 solution (2×100 ml). The organic phase was then cried over Na2SO4 and concentrated to give 2-fluoro-2-methylpropyl trifluoromethanesulfonate (12.89 g, 85%) as a red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09155727B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-09596fbf63b24ffa99e3afd778733aa7 |
| Source note | uspto-grants-2015_10 |