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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257025Generated: October 26, 2026

Water → N-(3-nitro-5-trifluoromethyl-2-pyridyl)methanesulfonamide

https://huagongshe.com/reaction/257025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantMethanesulfonamideHCID 72879—
Reactant2-Chloro-3-nitro-5-(trifluoromethyl)pyridineHCID 4736950—
SolventTetrahydrofuranHCID 8028—
ProductN-(3-nitro-5-trifluoromethyl-2-pyridyl)methanesulfonamideHCID 1080303465.8%

Reaction Steps

4.4 g of methanesulfonamide was dissolved in 70 ml of dry tetrahydrofuran, and 1.9 g of 60% sodium hydride was added thereto under cooling with ice. After completion of the addition, the mixture was reacted for one hour under reflux. After cooling, 7.0 g of 2-chloro-3-nitro-5-trifluoromethylpyridine was added thereto, and the mixture was reacted for 6 hours under reflux. After completion of the reaction, the reaction product was poured into 300 ml of water and washed with ethyl ether. Then, the aqueous layer was weakly acidified with dilute hydrochloric acid. Precipitated crystals were collected by filtration and dried to obtain 5.8 g of N-(3-nitro-5-trifluoromethyl-2-pyridyl)methanesulfonamide having a melting point of from 138° to 139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260320
Source datasetuspto-grants-1993_11
ORD IDord-c328a21511944f4aab1efc7a3f853101
Source noteuspto-grants-1993_11