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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184011Generated: October 25, 2026

Stannous chloride dihydrate → 2-Fluoro-2'-(methylthio)biphenyl-5-ylamine

https://huagongshe.com/reaction/2184011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
Reactant2-Fluoro-2'-methylthio-5-nitrobiphenylHCID 22285277—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-2'-(methylthio)biphenyl-5-ylamineHCID 2228529398%

Reaction Steps

A solution of 2-fluoro-2′-methylthio-5-nitrobiphenyl (6.00 g, 22.8 mmol) in tetrahydrofuran (50 ml) and ethanol (50 ml) was treated with tin(II) chloride dihydrate (25.70 g, 113.9 mmol) and the mixture was stirred at ambient temperature for 25 h. The solvent was evaporated and the residue stirred with 2N sodium hydroxide solution (240 ml) for 18 h. The resulting suspension was extracted with dichloromethane (3×200 ml). The combined organic extracts were dried over anhydrous magnesium sulphate and evaporated. The residue was purified by flash chromatography on silica gel eluting with 35% ethyl acetate in isohexane to afford 2-fluoro-2′-(methylthio)biphenyl-5-ylamine as a white solid (5.20 g, 98%): δH (360 MHz, CDCl3) 2.39 (3H, s), 6.60 (1H, dd, J 6 and 3), 6.64-6.68 (1H, m), 6.94 (1H, t, J 9), 7.19-7.20 (2H, m), 7.30 (1H, d, J 8), 7.33-7.37 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900215B2
Source datasetuspto-grants-2005_05
ORD IDord-bb5a349e83484d9982d7f125976cb86c
Source noteuspto-grants-2005_05