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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254944Generated: October 30, 2026

Methylamine → N-Methyl-3-nitrobenzenesulfonamide

https://huagongshe.com/reaction/254944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant3-Nitrobenzenesulfonyl chlorideHCID 8476—
SolventSodium ChlorideHCID 5234—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-Methyl-3-nitrobenzenesulfonamideHCID 579071—

Reaction Steps

To a solution of 4.42 g (20.0 mmol) of 3-nitrobenzenesulfonyl chloride in 150 mL of dry THF was added 25.0 mL (50.0 mmol) of methylamine as a 2 M solution in THF under ice cooling and stirring. The resulting cloudy solution was stirred overnight at ambient temperature. After this time period, the reaction mixture was diluted with 150 mL of saturated sodium chloride solution and 50 mL of ethyl acetate, then transferred to a 500 mL separatory funnel, mixed thoroughly, and the organic phase was separated. The aqueous phase was extracted twice with 50 mL of ethyl acetate. The combined organic layers were dried over Na2SO4, filtered, and concentrated under reduced pressure. The resulting residue was purified by recrytallization from EtOH. The yield of the title compound was 97% (4.20 g, 19.48 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875728B2
Source datasetuspto-grants-2011_01
ORD IDord-b20f259e9e8e4d1585dc7d55c7cb860b
Source noteuspto-grants-2011_01