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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427442Generated: November 2, 2026

2,6-Dimethyl-4-nitro-4'-(trifluoromethyl)biphenyl → 2,6-Dimethyl-4'-(trifluoromethyl)biphenyl-4-amine

https://huagongshe.com/reaction/1427442

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dimethyl-4-nitro-4'-(trifluoromethyl)biphenylHCID 67485659—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2,6-Dimethyl-4'-(trifluoromethyl)biphenyl-4-amineHCID 6748490489.1%

Reaction Steps

To a solution of 2,6-dimethyl-4-nitro-4′-(trifluoromethyl)biphenyl (600 mg, 2.03 mmol) in ethanol (20 mL) was added 10 wt % palladium on carbon (18 mg). The reaction was pressurized to 50 psi hydrogen and stirred at room temperature overnight. The reaction was filtered onto Celite and concentrated. Purification by column chromatography gave 2,6-dimethyl-4′-(trifluoromethyl)biphenyl-4-amine (480 mg, 89%) as a light yellow solid. 1H NMR (400 MHz, CDCl3, δ): 7.65 (d, 2H), 7.27 (s, 1H), 7.25 (s, 1H), 6.48 (s, 2H), 3.80 (s, 2H), 1.94 (s, 6H). MS (M+1): 266.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933104B2
Source datasetuspto-grants-2015_01
ORD IDord-12171385c2314a82bd97618e2548ac21
Source noteuspto-grants-2015_01