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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441757Generated: November 2, 2026

3-Nitro-5-(trifluoromethyl)benzoic acid → 3-Amino-5-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/1441757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitro-5-(trifluoromethyl)benzoic acidHCID 616602—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product3-Amino-5-(trifluoromethyl)benzoic acidHCID 609556—

Reaction Steps

A solution of 3-nitro-5-(trifluoromethyl)benzoic acid (Lancaster Synthesis GmbH; 11.75 g, 50 mmol) in ethanol (300 mL) is hydrogenated at atmospheric pressure over Raney nickel (1 g) at 40° C. The calculated amount of hydrogen is taken up after 8 hours. The mixture is then filtered and the solvent is evaporated off under reduced pressure to yield the crude product which is purified by recrystallisation from diethylether-hexane to give the title compound as a beige crystalline solid, m.p. 134-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655669B2
Source datasetuspto-grants-2010_02
ORD IDord-a470078fe6ba497fbca2b0aebfe76741
Source noteuspto-grants-2010_02