HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257029Generated: October 27, 2026
Acetic Acid → N-(3-amino-5-trifluoromethylethyl-2-pyridyl)ethanesulfonamide
https://huagongshe.com/reaction/257029
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | N-(3-nitro-5-trifluoromethyl-2-pyridyl)ethanesulfonamide | HCID 10851681 | — |
| Product | N-(3-amino-5-trifluoromethylethyl-2-pyridyl)ethanesulfonamide | HCID 67696611 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05260320 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-a56b632b05db48a18387ae97f6026afc |
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| Source note | uspto-grants-1993_11 |
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