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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226449Generated: October 31, 2026

Acetic Acid → N-(3-amino-5-trifluoromethylethyl-2-pyridyl)ethanesulfonamide

https://huagongshe.com/reaction/2226449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantN-(3-nitro-5-trifluoromethyl-2-pyridyl)ethanesulfonamideHCID 10851681—
ProductN-(3-amino-5-trifluoromethylethyl-2-pyridyl)ethanesulfonamideHCID 67696611—

Reaction Conditions

Temperature50 °C

Reaction Steps

3.0 g of N-(3-nitro-5-trifluoromethyl-2-pyridyl)ethanesulfonamide was suspended in a solvent mixture comprising 30 ml of water and 30 ml of acetic acid, and 2.2 g of reduced iron was added thereto. Then, the mixture was heated to 50° C. and reacted for one hour. After completion of the reaction, the reaction product was cooled to room temperature, and excess iron was separated by filtration. The filtrate was extracted with ethyl acetate. The extract layer was washed with water and dried. Ethyl acetate was distilled off under reduced pressure to obtain 2.5 g of N-(3-amino-5-trifluoromethylethyl-2-pyridyl)ethanesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05348967
Source datasetuspto-grants-1994_09
ORD IDord-1cda4e9a942047b8b2ee65c57dd88860
Source noteuspto-grants-1994_09