HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → N-Benzyl-N-(3,4-dimethoxy-phenyl)-4-fluoro-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(3,4-dimethoxyphenyl)-4-fluorobenzenesulfonamide | HCID 741636 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-Benzyl-N-(3,4-dimethoxy-phenyl)-4-fluoro-benzenesulfonamide | HCID 12051199 | 79.1% |
Reaction Steps
N-(3,4-Dimethoxy-phenyl)-4-fluoro-benzenesulfonamide (0.51 g, 1.61 mM) was added to a solution of benzyl bromide (0.57 g, 4.82 mM) and potassium carbonate (0.66 g, 4.82 mM)in anhyrous acetone(10 ml). The reaction was stirred overnight. The undissolved solids were removed by filtration and the mother liquor was concentrated. This gum was triturated with hexanes to afford 0.52 g of the desired product as an off-white solid. H1 NMR(CDCl3) δ 3.66(s, 3H), 3.81(s, 3H), 6.42(m, 2H), 6.66(d, 1H, J=8.70 Hz), 7.23(m, 7H), 7.71(m, 2H). MS(ES) m/z 401.9; (MH+); HRMS for C21H20SFNO4: 401.1094.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06743787B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-bd562a81dfc94262b2a009f77b52b428 |
| Source note | uspto-grants-2004_06 |