HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → 3,3,3-Trifluoropropyl trifluoromethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 3,3,3-Trifluoro-1-propanol | HCID 137512 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,3,3-Trifluoropropyl trifluoromethanesulfonate | HCID 14132849 | — |
Reaction Steps
To a cold (−25° C.) stirred solution of 2,6-lutidine (18.38 mL, 158 mmol) in DCM (120 mL) was added Tf2O (24.88 mL, 147 mmol) over 3 min, and the mixture was stirred for 5 min. To the reaction mixture was added 3,3,3-trifluoropropan-1-ol (12 g, 105 mmol) over an interval of 3 min. After 2 hr, the reaction mixture was warmed to room temperature and stirred for 1 hr. The reaction mixture was concentrated to half its volume, then purified by loading directly on a silica gel column (330 g ISCO) and the product was eluted with DCM to afford Intermediate S-1A (13.74 g, 53%) as a colorless oil. 1H NMR (400 MHz, CDCl3) δ ppm 4.71 (2H, t, J=6.15 Hz), 2.49-2.86 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273014B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-c0b862e28ffa4990afb01c7784743827 |
| Source note | uspto-grants-2016_03 |