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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173798Generated: October 31, 2026

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

https://huagongshe.com/reaction/2173798

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 numberUS09056834B2
Source datasetuspto-grants-2015_06
ORD IDord-95f31ef0c0a64bde88be4e375fdb04bb
Source noteuspto-grants-2015_06