HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748925Generated: October 26, 2026
Tert-Butylamine → N-t-Butyl 4-bromobenzenesulfonamide
https://huagongshe.com/reaction/748925
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-t-Butyl 4-bromobenzenesulfonamide | HCID 796629 | 86.2% |
Reaction Steps
Place t-butylamine (4.32 mL, 41.1 mmol), triethylamine (8.15 mL, 58.7 mmol) and dichloromethane (75 mL) in a 3-neck round bottom flask. Cool this stirring solution to 0° C. and add a solution of 4-bromobenzenesulfonyl chloride (10.0 g, 39.1 mmol) in dichloromethane (50 mL). Add additional dichloromethane (25 mL) and stir the reaction overnight, allowing it to warm to ambient temperature. Evaporate the reaction in vacuo. Suspend the resulting white solid in ethyl acetate and filter it. Concentrate the filtrate in vacuo and purify the resulting residue by flash chromatography (silica gel; 50%-80% gradient CH2Cl2 in hexanes) to provide 9.85 g of 4-bromo-N-tert-butyl-benzenesulfonamide (86%).
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-8d902a682dc54efdb5a5ca7f8fd1df48 |
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| Source note | uspto-grants-2008_07 |
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