HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → 4-Methylsulfanylthiophene-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 5-Trimethylsilyl-4-methylsulfanylthiophene-2-sulfonamide | HCID 22019476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Methylsulfanylthiophene-2-sulfonamide | HCID 22019495 | 82% |
Reaction Steps
To a solution of 5-trimethylsilyl-4-methylsulfanylthiophene-2-sulfonamide (660 mg, 2.34 mmol) in THF (10 mL) is added a solution of tetra-butylammonium fluoride (14.0 mL of 1 M in THF, 14.0 mmol). The reaction mixture is stirred at room temperature for 3 hr. The THF is removed under reduced pressure and the residue is dissolved in EtOAc (200 mL). The organic layer is washed with brine then dried (Na2SO4), filtered and concentrated in vacuo. The crude product is chromatographed on silica gel, eluting with Hex:EtOAc (2:1) to afford the title compound (400 mg, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084170B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-a67ac309ad074910a843d2a272c82903 |
| Source note | uspto-grants-2006_08 |