HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → N-(but-3-enyl)-2-nitro-N-phenylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | 2-Nitro-N-phenylbenzenesulfonamide | HCID 229600 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(but-3-enyl)-2-nitro-N-phenylbenzenesulfonamide | HCID 44131079 | 64.7% |
Reaction Steps
Crushed KOH (0.0484 g, 0.862 mmol, 1.2 equiv) was added to 2-nitro-N-phenylbenzenesulfonamide (0.200 g, 0.719 mmol) in 1 mL DMF, and the mixture was stirred for 30 min. 4-Bromo-1-butene (0.2426 g, 1.80 mmol) in 2 mL DMF solution was added dropwise into the mixture and it was stirred at room temperature overnight. The reaction mixture was diluted with 30 mL EtOAc and washed with 1M HCl 2×10 mL and water 3×10 mL. The organic layer was dried over anhydrous Na2SO4 and evaporated to afford the crude product, which was subjected to silica gel chromatography using Hexanes/EtOAc to afford 0.1546 g white solid, yield 63.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08748473B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-4d4033f98b6743cf940b1b8e318a7cfd |
| Source note | uspto-grants-2014_06 |