HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710336Generated: October 27, 2026
Potassium Carbonate → 4-bromo-N-(3-methoxyphenyl)-N-methylbenzenesulfonamide
https://huagongshe.com/reaction/710336
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-bromo-N-(3-methoxyphenyl)benzenesulfonamide | HCID 3361067 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-bromo-N-(3-methoxyphenyl)-N-methylbenzenesulfonamide | HCID 62003284 | — |
Reaction Steps
To a stirred solution of 4-bromo-N-(3-methoxyphenyl)benzenesulphonamide (0.5 g 1.46 mmol) and K2CO3 (0.5 g) in anhydrous DMF (7 ml) MeI (1 ml) was added and this was stirred at 50° C. for 0.5 h. The mixture was diluted to 50 ml with H2O and extracted in EtOAc (50 ml). The organic layer was washed with H2O, dried over MgSO4, filtered and the filtrate was passed through silica gel bead. The filtrate was evaporated to dryness to give the product (0.5 g; 96%), as a pale solid. 1H-NMR (CDCl3) 3.14 (5, 3H); 3.75 (s, 3H); 6.58 (broad d, 1H), 6.69 (t, 1H, J=2.20 Hz); 6.80 (dd, 1H, J=2.5, 8.34, Hz); 7.18 (tr, 1H, J=8.15 Hz); 7.40 (d, 2H, J=8.67 Hz); 7.58 (d, 2H, J=8.64 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181182B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-70dc8b915bbf4debb88057ea4877ba04 |
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| Source note | uspto-grants-2015_11 |
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