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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167121Generated: November 1, 2026

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

https://huagongshe.com/reaction/1167121

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) δ 3.66 (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 numberUS06617326B2
Source datasetuspto-grants-2003_09
ORD IDord-85b77720b3fb4174a2d838d356b5e04b
Source noteuspto-grants-2003_09