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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288307Generated: November 1, 2026

4-nitro-3-(trifluoromethyl)benzenesulfonamide → HCID 21482732, compound

https://huagongshe.com/reaction/1288307

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-nitro-3-(trifluoromethyl)benzenesulfonamideHCID 2778406—
ReactantHCID 178418361HCID 178418361—
CatalystRutheniumHCID 23950—
SolventEthanolHCID 702—
ProductHCID 21482732HCID 21482732—

Reaction Steps

1.0 G. of 4-nitro-3-trifluoromethylbenzenesulfonamide is hydrogenated over 5% Ruthenium on charcoal in 20 ml. of absolute ethanol at room temperature under 40 lbs. of hydrogen for 5 hours. The hydrogen uptake is 100% of theory. The mixture is filtered, evaporated and dried affording 0.87 g. of crude solid. This material is recrystallized from toluene affording 0.75 g. of 4-amino-3-trifluoromethylbenzenesulfonamide, m.p. 150° to 151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03987199
Source datasetuspto-grants-1976_10
ORD IDord-caf80078ef27423ebbba1078e8e7c7fa
Source noteuspto-grants-1976_10