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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183895Generated: November 2, 2026

Stannous chloride dihydrate → HCID 22473529, compound

https://huagongshe.com/reaction/2183895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
ReactantHCID 22473582HCID 22473582—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22473529HCID 22473529—

Reaction Steps

A cooled (0° C.) suspension of crude 4′-fluoro-3′-nitrobiphenyl-2-carbonitrile (10.7 g, 44 mmol) in ethanol (80 ml) and tetrahydrofuran (80 ml) was treated with tin(II) chloride dihydrate (29.8 g, 132 mmol) and this mixture was stirred at ambient temperature for 12 h. The solvent was removed in vacuo and the residue treated with ice-cold 2N sodium hydroxide (400 ml). The resulting slurry was stirred at ambient temperature for 60 min then extracted with dichloromethane (2×400 ml). The organics were combined, washed with water, brine, dried over anhydrous magnesium sulfate, filtered and pre-adsorbed onto silica. Purification by chromatography on silica gel eluting with isohexane on a gradient of ethyl acetate (5-40%) gave 3′-amino-4′-fluorobiphenyl-2-carbonitrile as a cream-coloured solid (4.3 g, 46% over 2 steps): δH (400 MHz, CDCl3) 3.85 (2H, br), 6.84 (1H, ddd, J 8, 4 and 2), 6.95 (1H, dd, J 8 and 2), 7.07 (1H, dd, J 11 and 8), 7.40-7.46 (2H, m), 7.57-7.62 (1H, m), 7.72-7.74 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900215B2
Source datasetuspto-grants-2005_05
ORD IDord-58206f07428648c7a34da88f529df948
Source noteuspto-grants-2005_05