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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061744Generated: November 2, 2026

Stannous chloride dihydrate → 5'-Amino-6,2'-difluorobiphenyl-2-carbonitrile

https://huagongshe.com/reaction/1061744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
Reactant6,2'-Difluoro-5'-nitrobiphenyl-2-carbonitrileHCID 11687542—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product5'-Amino-6,2'-difluorobiphenyl-2-carbonitrileHCID 11708427—

Reaction Steps

6,2′-Difluoro-5′-nitrobiphenyl-2-carbonitrile (3.25 g, 12.5 mmol) in tetrahydrofuran (20 mL) and ethanol (20 mL) was treated with tin(II) chloride dihydrate (9.86 g, 43.8 mmol) and the mixture left to stir at ambient temperature for 18 h. The solvent was evaporated and the residue stirred with 2 N sodium hydroxide solution (40 mL) for 2 h. The resulting suspension was diluted with water (100 mL) and extracted with dichloromethane (3×200 mL). The combined organics were washed with water (200 mL), brine (200 mL), dried over anhydrous sodium sulfate, filtered and evaporated to give 5′-amino-6,2′-difluorobiphenyl-2-carbonitrile as a brown oil (2.87 9,100%): δH (360 MHz, CDCl3) 3.74 (2H, s), 6.68 (1H, m), 6.73-6.77 (1H, m), 7.02 (1H, dd, J 9 and 9), 7.37-7.49 (2H, m), 7.56-7.65 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960598B2
Source datasetuspto-grants-2005_11
ORD IDord-234c04b2a95344f7adccbf88c6d76a32
Source noteuspto-grants-2005_11