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 | 70% |
Reaction Steps
Add trifluoromethanesulphonic anhydride (4.3 mL, 26.0 mmol) to a solution of 2-fluoro-2-methylpropan-1-ol (2.0 g, 21.7 mmol) and 2,6-lutidine (3.0 mL, 26.0 mmol) in dichloromethane (25 mL) at −78° C. Warm slowly to room temperature and stir at room temperature for 1 hour. Add water to quench the reaction, separate the organic layer and extract the aqueous layer with dichloromethane. Combine the organic layers, dry (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with dichloromethane), to give the desired compound as an oil (3.4 g, 70% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745438B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-e194009f2c234d79af1e5d5eb84cacb0 |
| Source note | uspto-grants-2010_06 |