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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393836Generated: November 1, 2026

N-[2-(4-nitroanilino)ethyl]methanesulfonamide → N-methyl-N-[2-(4-nitrophenylamino)ethyl]methanesulfonamide

https://huagongshe.com/reaction/1393836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[2-(4-nitroanilino)ethyl]methanesulfonamideHCID 2847338—
ReactantMethyl sulfate(1-)HCID 4694097—
SolventSodium HydroxideHCID 14798—
ProductN-methyl-N-[2-(4-nitrophenylamino)ethyl]methanesulfonamideHCID 2310446248.7%

Reaction Conditions

Temperature30 °C

Reaction Steps

25.9 g (0.1 mol) of N-[2-(4-nitrophenylamino)ethyl]methanesulfonamide (22) were dissolved in 200 mL of 1N sodium hydroxide at 50° C. The insoluble matter was filtered off, the filtrate was cooled to 30° C. and 11.4 mL (0.12 mol) of methyl sulfate were added dropwise. The mixture was stirred for 1 hour at room temperature and then heated to 40° C. and the yellow precipitate was filtered off. The product was reslurried in 0.5N sodium hydroxide and in water. The wet crude product was recrystallized from 50 mL of 96% ethanol with carbon black. 13.3 g of product with a melting point of 109° C. were isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07347879B2
Source datasetuspto-grants-2008_03
ORD IDord-bc3cf21ee81648e88a9a555567bdddee
Source noteuspto-grants-2008_03