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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890985Generated: November 1, 2026

Methylamine → N-methyl-1-(3-nitrophenyl)methanesulfonamide

https://huagongshe.com/reaction/1890985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant(3-Nitrophenyl)methanesulfonyl chlorideHCID 13196775—
SolventBenzeneHCID 241—
ProductN-methyl-1-(3-nitrophenyl)methanesulfonamideHCID 1328604690%

Reaction Steps

40% aqueous methylamine (10 mL, 0.1 mol) was added to a vigorously stirred solution of (3-Nitrophenyl)methanesulfonyl chloride (2.36 g, 10 mmol) in benzene (30 mL) and allowed to stir for 2 h at room temperature. To this end, the benzene layer was separated, and the aqueous layer extracted with CH2Cl2 (2×25 mL). The combined organic layers were washed with saturated aqueous NaHCO3 (30 mL), water (30 mL), filtered over anhydrous Na2SO4, filtered and the solvent removed under reduced pressure to give 2.07 g (90%) of (3-nitrophenyl)-N-methylmethanesulfonamide as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507498B2
Source datasetuspto-grants-2013_08
ORD IDord-754a9fb05f804bd99e1a4df8258c53bd
Source noteuspto-grants-2013_08