HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Fluorobenzenesulfonimide → HCID 118074105, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Fluorobenzenesulfonimide | HCID 588007 | — |
| Reactant | HCID 86714019 | HCID 86714019 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 118074105 | HCID 118074105 | — |
Reaction Steps
To a solution of the intermediate 17 (1.01 g, 1.2 mmol) in anhydrous THF (12.0 mL) were added dropwise n-BuLi (2.5M in hexane, 0.77 mL, 1.92 mmol) at −78° C. under nitrogen atmosphere, and the mixture was stirred for 20 min at the same temperature. Then a solution of N-fluorobenzenesulfonimide (0.68 g, 2.16 mmol) in THF (3.0 mL) was added dropwise, and the mixture was stirred for 1 h at the same temperature. The reaction mixture was quenched with saturated NaCl solution (10 mL) and extracted with EtOAc (50 mL). The organic layer was washed with brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo to provide the crude intermediate 19, which was used without further purification (0.95 g, 1.21 mmol, 101%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09034921B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-b0fefffe0f5744618c9e4363f128b4a1 |
| Source note | uspto-grants-2015_05 |