HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylmethylsulfonyl Fluoride → Potassium alpha-toluenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylmethylsulfonyl Fluoride | HCID 4784 | — |
| Reactant | Potassium trimethylsilanolate | HCID 23668039 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Potassium alpha-toluenesulfonate | HCID 23666503 | 58.3% |
Reaction Steps
The procedure of Example 1 was followed using α-toluenesulfonyl fluoride (2.0 g, 11.5 mmol) in dry tetrahydrofuran (15 mL), potassium trimethylsilanolate (1.48 g, 11.5 mmol) and dry tetrahydrofuran (45 mL), and 2 h of heating at reflux. Potassium α-toluenesulfonate (1.41 g, 58% yield) was isolated as a white solid: 1H NMR (D2O) δ 4.1 (s, CH2, 2H), 7.4 ppm (s, Ar--H's, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04723016 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-38f5d19da7814e449f56363466a7475c |
| Source note | uspto-grants-1988_02 |