HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748926Generated: October 30, 2026
Dimethylamine → 4-Bromo-N,N-dimethylbenzenesulphonamide
https://huagongshe.com/reaction/748926
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Bromo-N,N-dimethylbenzenesulphonamide | HCID 12818 | 97% |
Reaction Steps
Place dimethylamine (5.25 mL of a 2.0 M solution in THF, 10.4 mmol), triethylamine (2.04 mL, 14.68 mmol) and dichloromethane (30 mL) in a round bottom flask. Cool this solution to 0° C., while stirring, and add a solution of 4-bromobenzenesulfonyl-chloride (2.5 g, 9.78 mmol) in dichloromethane (30 mL); Add additional dichloromethane (10 mL) and stir the reaction overnight, letting it warm to ambient temperature. Concentrate the reaction in vacuo. Take up the resulting solid in ethyl acetate and filter. Evaporate the filtrate in vacuo and dry the resulting solid by vacuum to give 2.50 g of 4-bromo-N,N-dimethyl-benzenesulfonamide (97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07399867B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-49583e04f43e4484b4852483c7de5e51 |
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| Source note | uspto-grants-2008_07 |
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