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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17968Generated: October 25, 2026

Methylamine → 4-bromo-N-methylbenzene-1-sulfonamide

https://huagongshe.com/reaction/17968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product4-bromo-N-methylbenzene-1-sulfonamideHCID 10121596.8%

Reaction Conditions

Temperature20 °C

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, 4H), 4.62-4.78 (m, 1H), 2.65 (d, J=5.4 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741321B2
Source datasetuspto-grants-2010_06
ORD IDord-4ec898c1322241d9be83408d210eacfd
Source noteuspto-grants-2010_06