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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888258Generated: October 26, 2026

Hexane → [2-[2-[[3-(Trifluoromethyl)phenyl]sulfonyl]-ethylsulfanyl]-pyridin-3-yl]amine

https://huagongshe.com/reaction/888258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Nitro-2-[2-[[3-(trifluoromethyl)phenyl]sulfonyl]ethyl-sulfanyl]pyridineHCID 67133865—
CatalystZincHCID 23994—
SolventEthanolHCID 702—
Product[2-[2-[[3-(Trifluoromethyl)phenyl]sulfonyl]-ethylsulfanyl]-pyridin-3-yl]amineHCID 6713371376%

Reaction Conditions

Temperature0 °C

Reaction Steps

1.31 g (20 mmol) zinc was added to a solution of 1.96 g (5.0 mmol) 3-nitro-2-[2-[[3-(trifluoromethyl)phenyl]sulfonyl]ethyl-sulfanyl]pyridine in ethanol (45 ml) and the mixture was cooled to 0° C. 200 ml (0.2 M, 40 mmol) of an aqueous NH4Cl solution were added at this temperature and then the mixture was heated for 30 min at 90° C. Then the mixture was concentrated to small volume under vacuum and the residue was taken up with water and neutralised with NaHCO3. It was then extracted with EE and the organic phase was dried over Na2SO4, filtered and concentrated to small volume under vacuum. Column chromatography (hexane/EE 4:1) of the residue yielded 1.38 g (3.8 mmol, 76%) [2-[2-[[3-(trifluoromethyl)-phenyl]sulfonyl]-ethylsulfanyl]-pyridin-3-yl]amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247573B2
Source datasetuspto-grants-2012_08
ORD IDord-f375b2151ffd4c7badd07702ae9553e7
Source noteuspto-grants-2012_08