HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → 3,3,3-Trifluoropropyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3,3,3-Trifluoro-1-propanol | HCID 137512 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,3,3-Trifluoropropyl methanesulfonate | HCID 25210501 | 58.2% |
Reaction Steps
To a solution of 3,3,3-trifluoropropan-1-ol (500 mg, 4.38 mmol) in DCM (10 mL) was added TEA (1.22 mL, 8.77 mmol) followed by dropwise addition of methanesulfonyl chloride (0.51 mL, 6.58 mmol) at 0° C. The resulting mixture was stirred at room temperature for 2 h. The reaction was diluted with DCM and the organic phase washed with brine, dried and concentrated to give crude product which was purified via silica gel chromatography eluting with petroleum ether/ethyl acetate (5:1) to give 3,3,3-trifluoropropyl methanesulfonate (490 mg, 58.2% yield) as light yellow oil. TLC (petroleum ether/ethyl acetate=3:1), Rf=0.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09359359B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-a1aed81d00694da09b02c99e85dac7fa |
| Source note | uspto-grants-2016_06 |