HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 1-Bromo-2-p-tolylsulfonylacetylene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | p-Tolyl [2-(trimethylsilyl)ethynyl] sulfone | HCID 5075769 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Bromo-2-p-tolylsulfonylacetylene | HCID 10658911 | 96.5% |
Reaction Steps
To a stirred solution of trimethylsilyl p-tolylsulfonylacetylene (10 g, 40 mmol) in acetone (300 mL) was added silver nitrate (0.68 g, 4 mmol) followed by the addition of N-bromosuccinimide (7.6 g, 44 mmol) in one portion. The mixture was stirred at room temperature for 1 h. The resulting precipitate was filtered and washed with acetone. Silica gel (20 g) was added to the filtrate and the solvent was removed under reduced pressure. The residue was subjected to column chromatography with hexane/EtOAc (5:1) to afford the product as a light yellow solid (10 g, 96%). Mp. 99-101° C. 1H NMR (CDCl3) δ 7.87 (d, 2H, J=7.8 Hz), 7.39 (d, 2H, J=7.8 Hz), 2.47 (s, 3H); 13C NMR (CDCl3) δ 146.19, 138.16, 130.34, 127.83, 78.14, 61.70, 21.97.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030300B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-22a904764ac649dc935e1dafed2d5676 |
| Source note | uspto-grants-2011_10 |