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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226444Generated: November 2, 2026

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

https://huagongshe.com/reaction/2226444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantEthanesulfonamideHCID 73702—
Reactant2-Chloro-3-nitro-5-(trifluoromethyl)pyridineHCID 4736950—
SolventTetrahydrofuranHCID 8028—
ProductN-(3-nitro-5-trifluoromethyl-2-pyridyl)ethanesulfonamideHCID 1085168154.5%

Reaction Steps

3.1 g of ethanesulfonamide was dissolved in 50 ml of dry tetrahydrofuran, and 1.2 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, 5.0 g of 2-chloro-3-nitro-5-trifluoromethylpyridine was added thereto, and then the mixture was reacted for 7 hours under reflux. After completion of the reaction, the reaction product was poured into 200 ml of water. Undissolved materials in water were extracted with ethyl ether and removed. Then, the aqueous layer was weakly acidified with dilute hydrochloric acid. Precipitated crystals were collected by filtration and dried to obtain 3.6 g of N-(3-nitro-5-trifluoromethyl-2-pyridyl)ethanesulfonamide having a melting point of from 160° to 163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05348967
Source datasetuspto-grants-1994_09
ORD IDord-f5d56d8aee1e437992db16a5fd45e278
Source noteuspto-grants-1994_09