HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881127Generated: October 30, 2026
Methylamine → 4-bromo-N-methylbenzene-1-sulfonamide
https://huagongshe.com/reaction/881127
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-bromo-N-methylbenzene-1-sulfonamide | HCID 101215 | 96.8% |
Reaction Steps
To a mixture of sat aq. NaHCO3 (42 g, 0.5 mol), CH2Cl2 (400 mL) and methylamine (51.7 g, 0.5 mol, 30% in methanol) was added a solution of 4-bromo-benzenesulfonyl chloride (127 g, 0.5 mol) in CH2Cl2 (100 mL). The reaction was stirred at 20° C. overnight. The organic phase was separated and dried over Na2SO4. Evaporation of the solvent under reduced pressure provided the 4-bromo-N-methyl-benzenesulfonamide (121 g, crude), which was used in the next step without further purification. 1H NMR (CDCl3, 300 MHz) δ 7.64-7.74 (m, 4 H), 4.62-4.78 (m, 1 H), 2.65 (d, J=5.4 Hz, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993600B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-20d1550d457442d1b1a49ae02e83e4c6 |
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| Source note | uspto-grants-2015_03 |
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