HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4,4,5,5,5-Pentafluoropentyl 4-methylbenzenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4,4,5,5,5-Pentafluoropentan-1-ol | HCID 547967 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4,4,5,5,5-Pentafluoropentyl 4-methylbenzenesulfonate | HCID 22033027 | 91.4% |
Reaction Steps
A mixture of 4,4,5,5,5-pentafluoropentan-1-ol (1 g, 5.6 mmol), p-toluenesulfonylchloride (1.3 g, 6.8 mmol), and triethylamine (1.2 mL, 8.4 mmol) in DCM (20 mL) was stirred at room temperature for 18 h. Water was added to the reaction mixture, the two layers were separated, and the aqueous layer was extracted with DCM (2×). The organics were combined, dried over sodium sulfate, and evaporated to dryness. The residue was purified by column chromatography on silica gel eluting with 0 to 20% EtOAc/hexanes to afford 1.7 g of 4,4,5,5,5-pentafluoropentyl 4-methylbenzenesulfonate as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108944B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-45186e51e05b47b7a00aa3bd76654222 |
| Source note | uspto-grants-2015_08 |