HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586232Generated: October 28, 2026
4,2'-Difluoro-5'-nitrobiphenyl-2-carbonitrile → 5'-Amino-4,2'-difluorobiphenyl-2-carbonitrile
https://huagongshe.com/reaction/586232
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4,2'-Difluoro-5'-nitrobiphenyl-2-carbonitrile | HCID 11242411 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5'-Amino-4,2'-difluorobiphenyl-2-carbonitrile | HCID 11264703 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936608B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-9fa924521e6c4b3986a51cadf285f48a |
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| Source note | uspto-grants-2005_08 |
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