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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121372Generated: November 2, 2026

4,2'-Difluoro-5'-nitrobiphenyl-2-carbonitrile → 5'-Amino-4,2'-difluorobiphenyl-2-carbonitrile

https://huagongshe.com/reaction/2121372

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,2'-Difluoro-5'-nitrobiphenyl-2-carbonitrileHCID 11242411—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product5'-Amino-4,2'-difluorobiphenyl-2-carbonitrileHCID 11264703100%

Reaction Steps

A suspension of 4,2′-difluoro-5′-nitrobiphenyl-2-carbonitrile (26 g, 100 mmol) in ethanol (180 ml) and ethyl acetate (180 ml) was treated with platinum(IV) oxide (1.02 g, 4.5 mmol) and then shaken under an atmosphere of hydrogen (40 psi) for 1 h. [The reaction was very exothermic and complete solution is brought about by the increase in temperature]. The catalyst was removed by filtration through glass microfibre filter paper [if any crystalline product is present the filter cake is washed with dichloromethane] and the filtrate evaporated to dryness to afford 5′-amino-4,2′-difluorobiphenyl-2-carbonitrile as a straw-coloured solid (23 g, 100%): 1H NMR (360 MHz, CDCl3) δ3.66 (2H, s), 6.66-6.70 (1H, m), 6.71-6.74 (1H, m), 7.00 (1H, dd, J 9, 9 Hz), 7.33-7.38 (1H, m), 7.44-7.49 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696444B2
Source datasetuspto-grants-2004_02
ORD IDord-d285909ab9cc489886c34cc4b0a27f90
Source noteuspto-grants-2004_02